Canonical Allele Identifier: CA1506854246

Gene: RXFP1

Linked Data

• dbSNP Id: rs1771251744

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.158645096del , CM000666.2:g.158645096del	GRCh38
NC_000004.11:g.159566248del , CM000666.1:g.159566248del	GRCh37
NC_000004.10:g.159785698del	NCBI36
NG_031835.1:g.128383del
NG_031835.2:g.128383del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307765.10:c.1303del MANE Select	ENSP00000303248.5:p.Ser435LeufsTer19
ENST00000307765.9:c.1303del	ENSP00000303248.5:p.Ser435LeufsTer19
ENST00000342048.9:c.*913del	ENSP00000432036.1:n.*913del
ENST00000343542.9:c.1159del	ENSP00000345889.5:p.Ser387LeufsTer19
ENST00000423548.5:c.1384del	ENSP00000405841.2:p.Ser462LeufsTer19
ENST00000448688.6:c.835del	ENSP00000414885.3:p.Ser279LeufsTer19
ENST00000460056.6:c.1060del	ENSP00000423306.1:p.Ser354LeufsTer19
ENST00000470033.2:c.1204del	ENSP00000420712.1:p.Ser402LeufsTer19
ENST00000471616.5:c.1356del	ENSP00000434475.1:n.1356del
ENST00000613319.4:c.910del	ENSP00000480522.1:p.Ser304LeufsTer19
NM_001253727.1:c.1384del	NP_001240656.1:p.Ser462LeufsTer19
NM_001253728.1:c.1204del	NP_001240657.1:p.Ser402LeufsTer19
NM_001253729.1:c.1159del	NP_001240658.1:p.Ser387LeufsTer19
NM_001253730.1:c.910del	NP_001240659.1:p.Ser304LeufsTer19
NM_001253732.1:c.907del	NP_001240661.1:p.Ser303LeufsTer19
NM_001253733.1:c.835del	NP_001240662.1:p.Ser279LeufsTer19
NM_021634.3:c.1303del	NP_067647.2:p.Ser435LeufsTer19
NR_045579.1:n.2183del
NR_045580.1:n.1619del
NR_045581.1:n.1590del
NR_045582.1:n.1527del
NR_045583.1:n.1506del
NR_045584.1:n.1619del
XM_011532174.1:c.1381del	XP_011530476.1:p.Ser461LeufsTer19
XM_011532175.1:c.1312del	XP_011530477.1:p.Ser438LeufsTer19
XM_011532176.1:c.1231del	XP_011530478.1:p.Ser411LeufsTer19
XM_011532177.1:c.1141del	XP_011530479.1:p.Ser381LeufsTer19
XM_011532178.1:c.1141del	XP_011530480.1:p.Ser381LeufsTer19
XM_011532179.1:c.1196+5765del	XP_011530481.1:n.1196+5765del
NM_001363776.1:c.1060del	NP_001350705.1:p.Ser354LeufsTer19
XM_011532176.2:c.1231del	XP_011530478.1:p.Ser411LeufsTer19
XM_011532179.2:c.1196+5765del	XP_011530481.1:n.1196+5765del
XM_017008517.1:c.1309del	XP_016864006.1:p.Ser437LeufsTer19
XM_017008518.2:c.1300del	XP_016864007.1:p.Ser434LeufsTer19
XM_017008519.1:c.1141del	XP_016864008.1:p.Ser381LeufsTer19
XM_017008520.1:c.1141del	XP_016864009.1:p.Ser381LeufsTer19
XM_017008522.1:c.1057del	XP_016864011.1:p.Ser353LeufsTer19
XM_017008523.2:c.1115+5765del	XP_016864012.1:n.1115+5765del
XM_017008524.2:c.1043+5765del	XP_016864013.1:n.1043+5765del
XM_017008525.1:c.1016+5765del	XP_016864014.1:n.1016+5765del
XM_017008526.1:c.835del	XP_016864015.1:p.Ser279LeufsTer19
NM_021634.4:c.1303del MANE Select	NP_067647.2:p.Ser435LeufsTer19
NM_001253728.2:c.1204del	NP_001240657.1:p.Ser402LeufsTer19
NM_001253729.2:c.1159del	NP_001240658.1:p.Ser387LeufsTer19
NM_001253732.2:c.907del	NP_001240661.1:p.Ser303LeufsTer19
NR_045579.2:n.2015del
NR_045580.2:n.1451del
NR_045581.2:n.1422del
NR_045582.2:n.1359del
NR_045583.2:n.1338del
NR_045584.2:n.1451del
NM_001253727.2:c.1384del	NP_001240656.1:p.Ser462LeufsTer19
NM_001253730.2:c.910del	NP_001240659.1:p.Ser304LeufsTer19
NM_001253733.2:c.835del	NP_001240662.1:p.Ser279LeufsTer19