Canonical Allele Identifier: CA358564173

Gene: RXFP1

Linked Data

• MyVariant Identifiers: chr4:g.159566272T>A (hg19) ; chr4:g.158645120T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.158645120T>A , CM000666.2:g.158645120T>A	GRCh38
NC_000004.11:g.159566272T>A , CM000666.1:g.159566272T>A	GRCh37
NC_000004.10:g.159785722T>A	NCBI36
NG_031835.1:g.128407T>A
NG_031835.2:g.128407T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307765.10:c.1327T>A MANE Select	ENSP00000303248.5:p.Ser443Thr
ENST00000307765.9:c.1327T>A	ENSP00000303248.5:p.Ser443Thr
ENST00000342048.9:c.*937T>A	ENSP00000432036.1:n.*937T>A
ENST00000343542.9:c.1183T>A	ENSP00000345889.5:p.Ser395Thr
ENST00000423548.5:c.1408T>A	ENSP00000405841.2:p.Ser470Thr
ENST00000448688.6:c.859T>A	ENSP00000414885.3:p.Ser287Thr
ENST00000460056.6:c.1084T>A	ENSP00000423306.1:p.Ser362Thr
ENST00000470033.2:c.1228T>A	ENSP00000420712.1:p.Ser410Thr
ENST00000471616.5:c.1380T>A	ENSP00000434475.1:n.1380T>A
ENST00000613319.4:c.934T>A	ENSP00000480522.1:p.Ser312Thr
NM_001253727.1:c.1408T>A	NP_001240656.1:p.Ser470Thr
NM_001253728.1:c.1228T>A	NP_001240657.1:p.Ser410Thr
NM_001253729.1:c.1183T>A	NP_001240658.1:p.Ser395Thr
NM_001253730.1:c.934T>A	NP_001240659.1:p.Ser312Thr
NM_001253732.1:c.931T>A	NP_001240661.1:p.Ser311Thr
NM_001253733.1:c.859T>A	NP_001240662.1:p.Ser287Thr
NM_021634.3:c.1327T>A	NP_067647.2:p.Ser443Thr
NR_045579.1:n.2207T>A
NR_045580.1:n.1643T>A
NR_045581.1:n.1614T>A
NR_045582.1:n.1551T>A
NR_045583.1:n.1530T>A
NR_045584.1:n.1643T>A
XM_011532174.1:c.1405T>A	XP_011530476.1:p.Ser469Thr
XM_011532175.1:c.1336T>A	XP_011530477.1:p.Ser446Thr
XM_011532176.1:c.1255T>A	XP_011530478.1:p.Ser419Thr
XM_011532177.1:c.1165T>A	XP_011530479.1:p.Ser389Thr
XM_011532178.1:c.1165T>A	XP_011530480.1:p.Ser389Thr
XM_011532179.1:c.1196+5789T>A	XP_011530481.1:n.1196+5789T>A
NM_001363776.1:c.1084T>A	NP_001350705.1:p.Ser362Thr
XM_011532176.2:c.1255T>A	XP_011530478.1:p.Ser419Thr
XM_011532179.2:c.1196+5789T>A	XP_011530481.1:n.1196+5789T>A
XM_017008517.1:c.1333T>A	XP_016864006.1:p.Ser445Thr
XM_017008518.2:c.1324T>A	XP_016864007.1:p.Ser442Thr
XM_017008519.1:c.1165T>A	XP_016864008.1:p.Ser389Thr
XM_017008520.1:c.1165T>A	XP_016864009.1:p.Ser389Thr
XM_017008522.1:c.1081T>A	XP_016864011.1:p.Ser361Thr
XM_017008523.2:c.1115+5789T>A	XP_016864012.1:n.1115+5789T>A
XM_017008524.2:c.1043+5789T>A	XP_016864013.1:n.1043+5789T>A
XM_017008525.1:c.1016+5789T>A	XP_016864014.1:n.1016+5789T>A
XM_017008526.1:c.859T>A	XP_016864015.1:p.Ser287Thr
NM_021634.4:c.1327T>A MANE Select	NP_067647.2:p.Ser443Thr
NM_001253728.2:c.1228T>A	NP_001240657.1:p.Ser410Thr
NM_001253729.2:c.1183T>A	NP_001240658.1:p.Ser395Thr
NM_001253732.2:c.931T>A	NP_001240661.1:p.Ser311Thr
NR_045579.2:n.2039T>A
NR_045580.2:n.1475T>A
NR_045581.2:n.1446T>A
NR_045582.2:n.1383T>A
NR_045583.2:n.1362T>A
NR_045584.2:n.1475T>A
NM_001253727.2:c.1408T>A	NP_001240656.1:p.Ser470Thr
NM_001253730.2:c.934T>A	NP_001240659.1:p.Ser312Thr
NM_001253733.2:c.859T>A	NP_001240662.1:p.Ser287Thr