Canonical Allele Identifier: CA1506854256
Gene: RXFP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.158645132C= , CM000666.2:g.158645132C= GRCh38
NC_000004.11:g.159566284C= , CM000666.1:g.159566284C= GRCh37
NC_000004.10:g.159785734C= NCBI36
NG_031835.1:g.128419C=
NG_031835.2:g.128419C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307765.10:c.1339C= MANE Select ENSP00000303248.5:p.Leu447=
ENST00000307765.9:c.1339C= ENSP00000303248.5:p.Leu447=
ENST00000342048.9:c.*949C= ENSP00000432036.1:n.*949C=
ENST00000343542.9:c.1195C= ENSP00000345889.5:p.Leu399=
ENST00000423548.5:c.1420C= ENSP00000405841.2:p.Leu474=
ENST00000448688.6:c.871C= ENSP00000414885.3:p.Leu291=
ENST00000460056.6:c.1096C= ENSP00000423306.1:p.Leu366=
ENST00000470033.2:c.1240C= ENSP00000420712.1:p.Leu414=
ENST00000471616.5:c.1392C= ENSP00000434475.1:n.1392C=
ENST00000613319.4:c.946C= ENSP00000480522.1:p.Leu316=
NM_001253727.1:c.1420C= NP_001240656.1:p.Leu474=
NM_001253728.1:c.1240C= NP_001240657.1:p.Leu414=
NM_001253729.1:c.1195C= NP_001240658.1:p.Leu399=
NM_001253730.1:c.946C= NP_001240659.1:p.Leu316=
NM_001253732.1:c.943C= NP_001240661.1:p.Leu315=
NM_001253733.1:c.871C= NP_001240662.1:p.Leu291=
NM_021634.3:c.1339C= NP_067647.2:p.Leu447=
NR_045579.1:n.2219C=
NR_045580.1:n.1655C=
NR_045581.1:n.1626C=
NR_045582.1:n.1563C=
NR_045583.1:n.1542C=
NR_045584.1:n.1655C=
XM_011532174.1:c.1417C= XP_011530476.1:p.Leu473=
XM_011532175.1:c.1348C= XP_011530477.1:p.Leu450=
XM_011532176.1:c.1267C= XP_011530478.1:p.Leu423=
XM_011532177.1:c.1177C= XP_011530479.1:p.Leu393=
XM_011532178.1:c.1177C= XP_011530480.1:p.Leu393=
XM_011532179.1:c.1196+5801C= XP_011530481.1:n.1196+5801C=
NM_001363776.1:c.1096C= NP_001350705.1:p.Leu366=
XM_011532176.2:c.1267C= XP_011530478.1:p.Leu423=
XM_011532179.2:c.1196+5801C= XP_011530481.1:n.1196+5801C=
XM_017008517.1:c.1345C= XP_016864006.1:p.Leu449=
XM_017008518.2:c.1336C= XP_016864007.1:p.Leu446=
XM_017008519.1:c.1177C= XP_016864008.1:p.Leu393=
XM_017008520.1:c.1177C= XP_016864009.1:p.Leu393=
XM_017008522.1:c.1093C= XP_016864011.1:p.Leu365=
XM_017008523.2:c.1115+5801C= XP_016864012.1:n.1115+5801C=
XM_017008524.2:c.1043+5801C= XP_016864013.1:n.1043+5801C=
XM_017008525.1:c.1016+5801C= XP_016864014.1:n.1016+5801C=
XM_017008526.1:c.871C= XP_016864015.1:p.Leu291=
NM_021634.4:c.1339C= MANE Select NP_067647.2:p.Leu447=
NM_001253728.2:c.1240C= NP_001240657.1:p.Leu414=
NM_001253729.2:c.1195C= NP_001240658.1:p.Leu399=
NM_001253732.2:c.943C= NP_001240661.1:p.Leu315=
NR_045579.2:n.2051C=
NR_045580.2:n.1487C=
NR_045581.2:n.1458C=
NR_045582.2:n.1395C=
NR_045583.2:n.1374C=
NR_045584.2:n.1487C=
NM_001253727.2:c.1420C= NP_001240656.1:p.Leu474=
NM_001253730.2:c.946C= NP_001240659.1:p.Leu316=
NM_001253733.2:c.871C= NP_001240662.1:p.Leu291=