Canonical Allele Identifier: CA358564177

Gene: RXFP1

Linked Data

• MyVariant Identifiers: chr4:g.159566273C>G (hg19) ; chr4:g.158645121C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.158645121C>G , CM000666.2:g.158645121C>G	GRCh38
NC_000004.11:g.159566273C>G , CM000666.1:g.159566273C>G	GRCh37
NC_000004.10:g.159785723C>G	NCBI36
NG_031835.1:g.128408C>G
NG_031835.2:g.128408C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307765.10:c.1328C>G MANE Select	ENSP00000303248.5:p.Ser443Ter
ENST00000307765.9:c.1328C>G	ENSP00000303248.5:p.Ser443Ter
ENST00000342048.9:c.*938C>G	ENSP00000432036.1:n.*938C>G
ENST00000343542.9:c.1184C>G	ENSP00000345889.5:p.Ser395Ter
ENST00000423548.5:c.1409C>G	ENSP00000405841.2:p.Ser470Ter
ENST00000448688.6:c.860C>G	ENSP00000414885.3:p.Ser287Ter
ENST00000460056.6:c.1085C>G	ENSP00000423306.1:p.Ser362Ter
ENST00000470033.2:c.1229C>G	ENSP00000420712.1:p.Ser410Ter
ENST00000471616.5:c.1381C>G	ENSP00000434475.1:n.1381C>G
ENST00000613319.4:c.935C>G	ENSP00000480522.1:p.Ser312Ter
NM_001253727.1:c.1409C>G	NP_001240656.1:p.Ser470Ter
NM_001253728.1:c.1229C>G	NP_001240657.1:p.Ser410Ter
NM_001253729.1:c.1184C>G	NP_001240658.1:p.Ser395Ter
NM_001253730.1:c.935C>G	NP_001240659.1:p.Ser312Ter
NM_001253732.1:c.932C>G	NP_001240661.1:p.Ser311Ter
NM_001253733.1:c.860C>G	NP_001240662.1:p.Ser287Ter
NM_021634.3:c.1328C>G	NP_067647.2:p.Ser443Ter
NR_045579.1:n.2208C>G
NR_045580.1:n.1644C>G
NR_045581.1:n.1615C>G
NR_045582.1:n.1552C>G
NR_045583.1:n.1531C>G
NR_045584.1:n.1644C>G
XM_011532174.1:c.1406C>G	XP_011530476.1:p.Ser469Ter
XM_011532175.1:c.1337C>G	XP_011530477.1:p.Ser446Ter
XM_011532176.1:c.1256C>G	XP_011530478.1:p.Ser419Ter
XM_011532177.1:c.1166C>G	XP_011530479.1:p.Ser389Ter
XM_011532178.1:c.1166C>G	XP_011530480.1:p.Ser389Ter
XM_011532179.1:c.1196+5790C>G	XP_011530481.1:n.1196+5790C>G
NM_001363776.1:c.1085C>G	NP_001350705.1:p.Ser362Ter
XM_011532176.2:c.1256C>G	XP_011530478.1:p.Ser419Ter
XM_011532179.2:c.1196+5790C>G	XP_011530481.1:n.1196+5790C>G
XM_017008517.1:c.1334C>G	XP_016864006.1:p.Ser445Ter
XM_017008518.2:c.1325C>G	XP_016864007.1:p.Ser442Ter
XM_017008519.1:c.1166C>G	XP_016864008.1:p.Ser389Ter
XM_017008520.1:c.1166C>G	XP_016864009.1:p.Ser389Ter
XM_017008522.1:c.1082C>G	XP_016864011.1:p.Ser361Ter
XM_017008523.2:c.1115+5790C>G	XP_016864012.1:n.1115+5790C>G
XM_017008524.2:c.1043+5790C>G	XP_016864013.1:n.1043+5790C>G
XM_017008525.1:c.1016+5790C>G	XP_016864014.1:n.1016+5790C>G
XM_017008526.1:c.860C>G	XP_016864015.1:p.Ser287Ter
NM_021634.4:c.1328C>G MANE Select	NP_067647.2:p.Ser443Ter
NM_001253728.2:c.1229C>G	NP_001240657.1:p.Ser410Ter
NM_001253729.2:c.1184C>G	NP_001240658.1:p.Ser395Ter
NM_001253732.2:c.932C>G	NP_001240661.1:p.Ser311Ter
NR_045579.2:n.2040C>G
NR_045580.2:n.1476C>G
NR_045581.2:n.1447C>G
NR_045582.2:n.1384C>G
NR_045583.2:n.1363C>G
NR_045584.2:n.1476C>G
NM_001253727.2:c.1409C>G	NP_001240656.1:p.Ser470Ter
NM_001253730.2:c.935C>G	NP_001240659.1:p.Ser312Ter
NM_001253733.2:c.860C>G	NP_001240662.1:p.Ser287Ter