Canonical Allele Identifier: CA1506854261

Gene: RXFP1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.158645142_158645152delinsAGTATTTCCTG , CM000666.2:g.158645142_158645152delinsAGTATTTCCTG	GRCh38
NC_000004.11:g.159566294_159566304delinsAGTATTTCCTG , CM000666.1:g.159566294_159566304delinsAGTATTTCCTG	GRCh37
NC_000004.10:g.159785744_159785754delinsAGTATTTCCTG	NCBI36
NG_031835.1:g.128429_128439delinsAGTATTTCCTG
NG_031835.2:g.128429_128439delinsAGTATTTCCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307765.10:c.1345+4_1345+14delinsAGTATTTCCTG MANE Select	ENSP00000303248.5:n.1345+4_1345+14delinsAGTATTTCCTG
ENST00000307765.9:c.1345+4_1345+14delinsAGTATTTCCTG	ENSP00000303248.5:n.1345+4_1345+14delinsAGTATTTCCTG
ENST00000342048.9:c.*955+4_*955+14delinsAGTATTTCCTG	ENSP00000432036.1:n.*955+4_*955+14delinsAGTATTTCCTG
ENST00000343542.9:c.1201+4_1201+14delinsAGTATTTCCTG	ENSP00000345889.5:n.1201+4_1201+14delinsAGTATTTCCTG
ENST00000423548.5:c.1426+4_1426+14delinsAGTATTTCCTG	ENSP00000405841.2:n.1426+4_1426+14delinsAGTATTTCCTG
ENST00000448688.6:c.877+4_877+14delinsAGTATTTCCTG	ENSP00000414885.3:n.877+4_877+14delinsAGTATTTCCTG
ENST00000460056.6:c.1102+4_1102+14delinsAGTATTTCCTG	ENSP00000423306.1:n.1102+4_1102+14delinsAGTATTTCCTG
ENST00000470033.2:c.1246+4_1246+14delinsAGTATTTCCTG	ENSP00000420712.1:n.1246+4_1246+14delinsAGTATTTCCTG
ENST00000471616.5:c.1398+4_1398+14delinsAGTATTTCCTG	ENSP00000434475.1:n.1398+4_1398+14delinsAGTATTTCCTG
ENST00000613319.4:c.952+4_952+14delinsAGTATTTCCTG	ENSP00000480522.1:n.952+4_952+14delinsAGTATTTCCTG
NM_001253727.1:c.1426+4_1426+14delinsAGTATTTCCTG	NP_001240656.1:n.1426+4_1426+14delinsAGTATTTCCTG
NM_001253728.1:c.1246+4_1246+14delinsAGTATTTCCTG	NP_001240657.1:n.1246+4_1246+14delinsAGTATTTCCTG
NM_001253729.1:c.1201+4_1201+14delinsAGTATTTCCTG	NP_001240658.1:n.1201+4_1201+14delinsAGTATTTCCTG
NM_001253730.1:c.952+4_952+14delinsAGTATTTCCTG	NP_001240659.1:n.952+4_952+14delinsAGTATTTCCTG
NM_001253732.1:c.949+4_949+14delinsAGTATTTCCTG	NP_001240661.1:n.949+4_949+14delinsAGTATTTCCTG
NM_001253733.1:c.877+4_877+14delinsAGTATTTCCTG	NP_001240662.1:n.877+4_877+14delinsAGTATTTCCTG
NM_021634.3:c.1345+4_1345+14delinsAGTATTTCCTG	NP_067647.2:n.1345+4_1345+14delinsAGTATTTCCTG
NR_045579.1:n.2225+4_2225+14delinsAGTATTTCCTG
NR_045580.1:n.1661+4_1661+14delinsAGTATTTCCTG
NR_045581.1:n.1632+4_1632+14delinsAGTATTTCCTG
NR_045582.1:n.1569+4_1569+14delinsAGTATTTCCTG
NR_045583.1:n.1548+4_1548+14delinsAGTATTTCCTG
NR_045584.1:n.1661+4_1661+14delinsAGTATTTCCTG
XM_011532174.1:c.1423+4_1423+14delinsAGTATTTCCTG	XP_011530476.1:n.1423+4_1423+14delinsAGTATTTCCTG
XM_011532175.1:c.1354+4_1354+14delinsAGTATTTCCTG	XP_011530477.1:n.1354+4_1354+14delinsAGTATTTCCTG
XM_011532176.1:c.1273+4_1273+14delinsAGTATTTCCTG	XP_011530478.1:n.1273+4_1273+14delinsAGTATTTCCTG
XM_011532177.1:c.1183+4_1183+14delinsAGTATTTCCTG	XP_011530479.1:n.1183+4_1183+14delinsAGTATTTCCTG
XM_011532178.1:c.1183+4_1183+14delinsAGTATTTCCTG	XP_011530480.1:n.1183+4_1183+14delinsAGTATTTCCTG
XM_011532179.1:c.1196+5811_1196+5821delinsAGTATTTCCTG	XP_011530481.1:n.1196+5811_1196+5821delinsAGTATTTCCTG
NM_001363776.1:c.1102+4_1102+14delinsAGTATTTCCTG	NP_001350705.1:n.1102+4_1102+14delinsAGTATTTCCTG
XM_011532176.2:c.1273+4_1273+14delinsAGTATTTCCTG	XP_011530478.1:n.1273+4_1273+14delinsAGTATTTCCTG
XM_011532179.2:c.1196+5811_1196+5821delinsAGTATTTCCTG	XP_011530481.1:n.1196+5811_1196+5821delinsAGTATTTCCTG
XM_017008517.1:c.1351+4_1351+14delinsAGTATTTCCTG	XP_016864006.1:n.1351+4_1351+14delinsAGTATTTCCTG
XM_017008518.2:c.1342+4_1342+14delinsAGTATTTCCTG	XP_016864007.1:n.1342+4_1342+14delinsAGTATTTCCTG
XM_017008519.1:c.1183+4_1183+14delinsAGTATTTCCTG	XP_016864008.1:n.1183+4_1183+14delinsAGTATTTCCTG
XM_017008520.1:c.1183+4_1183+14delinsAGTATTTCCTG	XP_016864009.1:n.1183+4_1183+14delinsAGTATTTCCTG
XM_017008522.1:c.1099+4_1099+14delinsAGTATTTCCTG	XP_016864011.1:n.1099+4_1099+14delinsAGTATTTCCTG
XM_017008523.2:c.1115+5811_1115+5821delinsAGTATTTCCTG	XP_016864012.1:n.1115+5811_1115+5821delinsAGTATTTCCTG
XM_017008524.2:c.1043+5811_1043+5821delinsAGTATTTCCTG	XP_016864013.1:n.1043+5811_1043+5821delinsAGTATTTCCTG
XM_017008525.1:c.1016+5811_1016+5821delinsAGTATTTCCTG	XP_016864014.1:n.1016+5811_1016+5821delinsAGTATTTCCTG
XM_017008526.1:c.877+4_877+14delinsAGTATTTCCTG	XP_016864015.1:n.877+4_877+14delinsAGTATTTCCTG
NM_021634.4:c.1345+4_1345+14delinsAGTATTTCCTG MANE Select	NP_067647.2:n.1345+4_1345+14delinsAGTATTTCCTG
NM_001253728.2:c.1246+4_1246+14delinsAGTATTTCCTG	NP_001240657.1:n.1246+4_1246+14delinsAGTATTTCCTG
NM_001253729.2:c.1201+4_1201+14delinsAGTATTTCCTG	NP_001240658.1:n.1201+4_1201+14delinsAGTATTTCCTG
NM_001253732.2:c.949+4_949+14delinsAGTATTTCCTG	NP_001240661.1:n.949+4_949+14delinsAGTATTTCCTG
NR_045579.2:n.2057+4_2057+14delinsAGTATTTCCTG
NR_045580.2:n.1493+4_1493+14delinsAGTATTTCCTG
NR_045581.2:n.1464+4_1464+14delinsAGTATTTCCTG
NR_045582.2:n.1401+4_1401+14delinsAGTATTTCCTG
NR_045583.2:n.1380+4_1380+14delinsAGTATTTCCTG
NR_045584.2:n.1493+4_1493+14delinsAGTATTTCCTG
NM_001253727.2:c.1426+4_1426+14delinsAGTATTTCCTG	NP_001240656.1:n.1426+4_1426+14delinsAGTATTTCCTG
NM_001253730.2:c.952+4_952+14delinsAGTATTTCCTG	NP_001240659.1:n.952+4_952+14delinsAGTATTTCCTG
NM_001253733.2:c.877+4_877+14delinsAGTATTTCCTG	NP_001240662.1:n.877+4_877+14delinsAGTATTTCCTG