Canonical Allele Identifier: CA1506854317

Gene: RXFP1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.158645249_158645250delinsCT , CM000666.2:g.158645249_158645250delinsCT	GRCh38
NC_000004.11:g.159566401_159566402delinsCT , CM000666.1:g.159566401_159566402delinsCT	GRCh37
NC_000004.10:g.159785851_159785852delinsCT	NCBI36
NG_031835.1:g.128536_128537delinsCT
NG_031835.2:g.128536_128537delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307765.10:c.1345+111_1345+112delinsCT MANE Select	ENSP00000303248.5:n.1345+111_1345+112delinsCT
ENST00000307765.9:c.1345+111_1345+112delinsCT	ENSP00000303248.5:n.1345+111_1345+112delinsCT
ENST00000342048.9:c.*955+111_*955+112delinsCT	ENSP00000432036.1:n.*955+111_*955+112delinsCT
ENST00000343542.9:c.1201+111_1201+112delinsCT	ENSP00000345889.5:n.1201+111_1201+112delinsCT
ENST00000423548.5:c.1426+111_1426+112delinsCT	ENSP00000405841.2:n.1426+111_1426+112delinsCT
ENST00000448688.6:c.877+111_877+112delinsCT	ENSP00000414885.3:n.877+111_877+112delinsCT
ENST00000460056.6:c.1102+111_1102+112delinsCT	ENSP00000423306.1:n.1102+111_1102+112delinsCT
ENST00000470033.2:c.1246+111_1246+112delinsCT	ENSP00000420712.1:n.1246+111_1246+112delinsCT
ENST00000471616.5:c.1398+111_1398+112delinsCT	ENSP00000434475.1:n.1398+111_1398+112delinsCT
ENST00000613319.4:c.952+111_952+112delinsCT	ENSP00000480522.1:n.952+111_952+112delinsCT
NM_001253727.1:c.1426+111_1426+112delinsCT	NP_001240656.1:n.1426+111_1426+112delinsCT
NM_001253728.1:c.1246+111_1246+112delinsCT	NP_001240657.1:n.1246+111_1246+112delinsCT
NM_001253729.1:c.1201+111_1201+112delinsCT	NP_001240658.1:n.1201+111_1201+112delinsCT
NM_001253730.1:c.952+111_952+112delinsCT	NP_001240659.1:n.952+111_952+112delinsCT
NM_001253732.1:c.949+111_949+112delinsCT	NP_001240661.1:n.949+111_949+112delinsCT
NM_001253733.1:c.877+111_877+112delinsCT	NP_001240662.1:n.877+111_877+112delinsCT
NM_021634.3:c.1345+111_1345+112delinsCT	NP_067647.2:n.1345+111_1345+112delinsCT
NR_045579.1:n.2225+111_2225+112delinsCT
NR_045580.1:n.1661+111_1661+112delinsCT
NR_045581.1:n.1632+111_1632+112delinsCT
NR_045582.1:n.1569+111_1569+112delinsCT
NR_045583.1:n.1548+111_1548+112delinsCT
NR_045584.1:n.1661+111_1661+112delinsCT
XM_011532174.1:c.1423+111_1423+112delinsCT	XP_011530476.1:n.1423+111_1423+112delinsCT
XM_011532175.1:c.1354+111_1354+112delinsCT	XP_011530477.1:n.1354+111_1354+112delinsCT
XM_011532176.1:c.1273+111_1273+112delinsCT	XP_011530478.1:n.1273+111_1273+112delinsCT
XM_011532177.1:c.1183+111_1183+112delinsCT	XP_011530479.1:n.1183+111_1183+112delinsCT
XM_011532178.1:c.1183+111_1183+112delinsCT	XP_011530480.1:n.1183+111_1183+112delinsCT
XM_011532179.1:c.1196+5918_1196+5919delinsCT	XP_011530481.1:n.1196+5918_1196+5919delinsCT
NM_001363776.1:c.1102+111_1102+112delinsCT	NP_001350705.1:n.1102+111_1102+112delinsCT
XM_011532176.2:c.1273+111_1273+112delinsCT	XP_011530478.1:n.1273+111_1273+112delinsCT
XM_011532179.2:c.1196+5918_1196+5919delinsCT	XP_011530481.1:n.1196+5918_1196+5919delinsCT
XM_017008517.1:c.1351+111_1351+112delinsCT	XP_016864006.1:n.1351+111_1351+112delinsCT
XM_017008518.2:c.1342+111_1342+112delinsCT	XP_016864007.1:n.1342+111_1342+112delinsCT
XM_017008519.1:c.1183+111_1183+112delinsCT	XP_016864008.1:n.1183+111_1183+112delinsCT
XM_017008520.1:c.1183+111_1183+112delinsCT	XP_016864009.1:n.1183+111_1183+112delinsCT
XM_017008522.1:c.1099+111_1099+112delinsCT	XP_016864011.1:n.1099+111_1099+112delinsCT
XM_017008523.2:c.1115+5918_1115+5919delinsCT	XP_016864012.1:n.1115+5918_1115+5919delinsCT
XM_017008524.2:c.1043+5918_1043+5919delinsCT	XP_016864013.1:n.1043+5918_1043+5919delinsCT
XM_017008525.1:c.1016+5918_1016+5919delinsCT	XP_016864014.1:n.1016+5918_1016+5919delinsCT
XM_017008526.1:c.877+111_877+112delinsCT	XP_016864015.1:n.877+111_877+112delinsCT
NM_021634.4:c.1345+111_1345+112delinsCT MANE Select	NP_067647.2:n.1345+111_1345+112delinsCT
NM_001253728.2:c.1246+111_1246+112delinsCT	NP_001240657.1:n.1246+111_1246+112delinsCT
NM_001253729.2:c.1201+111_1201+112delinsCT	NP_001240658.1:n.1201+111_1201+112delinsCT
NM_001253732.2:c.949+111_949+112delinsCT	NP_001240661.1:n.949+111_949+112delinsCT
NR_045579.2:n.2057+111_2057+112delinsCT
NR_045580.2:n.1493+111_1493+112delinsCT
NR_045581.2:n.1464+111_1464+112delinsCT
NR_045582.2:n.1401+111_1401+112delinsCT
NR_045583.2:n.1380+111_1380+112delinsCT
NR_045584.2:n.1493+111_1493+112delinsCT
NM_001253727.2:c.1426+111_1426+112delinsCT	NP_001240656.1:n.1426+111_1426+112delinsCT
NM_001253730.2:c.952+111_952+112delinsCT	NP_001240659.1:n.952+111_952+112delinsCT
NM_001253733.2:c.877+111_877+112delinsCT	NP_001240662.1:n.877+111_877+112delinsCT