Canonical Allele Identifier: CA1506854349

Gene: RXFP1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.158645319_158645320delinsGT , CM000666.2:g.158645319_158645320delinsGT	GRCh38
NC_000004.11:g.159566471_159566472delinsGT , CM000666.1:g.159566471_159566472delinsGT	GRCh37
NC_000004.10:g.159785921_159785922delinsGT	NCBI36
NG_031835.1:g.128606_128607delinsGT
NG_031835.2:g.128606_128607delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307765.10:c.1345+181_1345+182delinsGT MANE Select	ENSP00000303248.5:n.1345+181_1345+182delinsGT
ENST00000307765.9:c.1345+181_1345+182delinsGT	ENSP00000303248.5:n.1345+181_1345+182delinsGT
ENST00000342048.9:c.*955+181_*955+182delinsGT	ENSP00000432036.1:n.*955+181_*955+182delinsGT
ENST00000343542.9:c.1201+181_1201+182delinsGT	ENSP00000345889.5:n.1201+181_1201+182delinsGT
ENST00000423548.5:c.1426+181_1426+182delinsGT	ENSP00000405841.2:n.1426+181_1426+182delinsGT
ENST00000448688.6:c.877+181_877+182delinsGT	ENSP00000414885.3:n.877+181_877+182delinsGT
ENST00000460056.6:c.1102+181_1102+182delinsGT	ENSP00000423306.1:n.1102+181_1102+182delinsGT
ENST00000470033.2:c.1246+181_1246+182delinsGT	ENSP00000420712.1:n.1246+181_1246+182delinsGT
ENST00000471616.5:c.1398+181_1398+182delinsGT	ENSP00000434475.1:n.1398+181_1398+182delinsGT
ENST00000613319.4:c.952+181_952+182delinsGT	ENSP00000480522.1:n.952+181_952+182delinsGT
NM_001253727.1:c.1426+181_1426+182delinsGT	NP_001240656.1:n.1426+181_1426+182delinsGT
NM_001253728.1:c.1246+181_1246+182delinsGT	NP_001240657.1:n.1246+181_1246+182delinsGT
NM_001253729.1:c.1201+181_1201+182delinsGT	NP_001240658.1:n.1201+181_1201+182delinsGT
NM_001253730.1:c.952+181_952+182delinsGT	NP_001240659.1:n.952+181_952+182delinsGT
NM_001253732.1:c.949+181_949+182delinsGT	NP_001240661.1:n.949+181_949+182delinsGT
NM_001253733.1:c.877+181_877+182delinsGT	NP_001240662.1:n.877+181_877+182delinsGT
NM_021634.3:c.1345+181_1345+182delinsGT	NP_067647.2:n.1345+181_1345+182delinsGT
NR_045579.1:n.2225+181_2225+182delinsGT
NR_045580.1:n.1661+181_1661+182delinsGT
NR_045581.1:n.1632+181_1632+182delinsGT
NR_045582.1:n.1569+181_1569+182delinsGT
NR_045583.1:n.1548+181_1548+182delinsGT
NR_045584.1:n.1661+181_1661+182delinsGT
XM_011532174.1:c.1423+181_1423+182delinsGT	XP_011530476.1:n.1423+181_1423+182delinsGT
XM_011532175.1:c.1354+181_1354+182delinsGT	XP_011530477.1:n.1354+181_1354+182delinsGT
XM_011532176.1:c.1273+181_1273+182delinsGT	XP_011530478.1:n.1273+181_1273+182delinsGT
XM_011532177.1:c.1183+181_1183+182delinsGT	XP_011530479.1:n.1183+181_1183+182delinsGT
XM_011532178.1:c.1183+181_1183+182delinsGT	XP_011530480.1:n.1183+181_1183+182delinsGT
XM_011532179.1:c.1196+5988_1196+5989delinsGT	XP_011530481.1:n.1196+5988_1196+5989delinsGT
NM_001363776.1:c.1102+181_1102+182delinsGT	NP_001350705.1:n.1102+181_1102+182delinsGT
XM_011532176.2:c.1273+181_1273+182delinsGT	XP_011530478.1:n.1273+181_1273+182delinsGT
XM_011532179.2:c.1196+5988_1196+5989delinsGT	XP_011530481.1:n.1196+5988_1196+5989delinsGT
XM_017008517.1:c.1351+181_1351+182delinsGT	XP_016864006.1:n.1351+181_1351+182delinsGT
XM_017008518.2:c.1342+181_1342+182delinsGT	XP_016864007.1:n.1342+181_1342+182delinsGT
XM_017008519.1:c.1183+181_1183+182delinsGT	XP_016864008.1:n.1183+181_1183+182delinsGT
XM_017008520.1:c.1183+181_1183+182delinsGT	XP_016864009.1:n.1183+181_1183+182delinsGT
XM_017008522.1:c.1099+181_1099+182delinsGT	XP_016864011.1:n.1099+181_1099+182delinsGT
XM_017008523.2:c.1115+5988_1115+5989delinsGT	XP_016864012.1:n.1115+5988_1115+5989delinsGT
XM_017008524.2:c.1043+5988_1043+5989delinsGT	XP_016864013.1:n.1043+5988_1043+5989delinsGT
XM_017008525.1:c.1016+5988_1016+5989delinsGT	XP_016864014.1:n.1016+5988_1016+5989delinsGT
XM_017008526.1:c.877+181_877+182delinsGT	XP_016864015.1:n.877+181_877+182delinsGT
NM_021634.4:c.1345+181_1345+182delinsGT MANE Select	NP_067647.2:n.1345+181_1345+182delinsGT
NM_001253728.2:c.1246+181_1246+182delinsGT	NP_001240657.1:n.1246+181_1246+182delinsGT
NM_001253729.2:c.1201+181_1201+182delinsGT	NP_001240658.1:n.1201+181_1201+182delinsGT
NM_001253732.2:c.949+181_949+182delinsGT	NP_001240661.1:n.949+181_949+182delinsGT
NR_045579.2:n.2057+181_2057+182delinsGT
NR_045580.2:n.1493+181_1493+182delinsGT
NR_045581.2:n.1464+181_1464+182delinsGT
NR_045582.2:n.1401+181_1401+182delinsGT
NR_045583.2:n.1380+181_1380+182delinsGT
NR_045584.2:n.1493+181_1493+182delinsGT
NM_001253727.2:c.1426+181_1426+182delinsGT	NP_001240656.1:n.1426+181_1426+182delinsGT
NM_001253730.2:c.952+181_952+182delinsGT	NP_001240659.1:n.952+181_952+182delinsGT
NM_001253733.2:c.877+181_877+182delinsGT	NP_001240662.1:n.877+181_877+182delinsGT