Canonical Allele Identifier: CA358564182

Gene: RXFP1

Linked Data

• MyVariant Identifiers: chr4:g.159566276T>A (hg19) ; chr4:g.158645124T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.158645124T>A , CM000666.2:g.158645124T>A	GRCh38
NC_000004.11:g.159566276T>A , CM000666.1:g.159566276T>A	GRCh37
NC_000004.10:g.159785726T>A	NCBI36
NG_031835.1:g.128411T>A
NG_031835.2:g.128411T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307765.10:c.1331T>A MANE Select	ENSP00000303248.5:p.Ile444Asn
ENST00000307765.9:c.1331T>A	ENSP00000303248.5:p.Ile444Asn
ENST00000342048.9:c.*941T>A	ENSP00000432036.1:n.*941T>A
ENST00000343542.9:c.1187T>A	ENSP00000345889.5:p.Ile396Asn
ENST00000423548.5:c.1412T>A	ENSP00000405841.2:p.Ile471Asn
ENST00000448688.6:c.863T>A	ENSP00000414885.3:p.Ile288Asn
ENST00000460056.6:c.1088T>A	ENSP00000423306.1:p.Ile363Asn
ENST00000470033.2:c.1232T>A	ENSP00000420712.1:p.Ile411Asn
ENST00000471616.5:c.1384T>A	ENSP00000434475.1:n.1384T>A
ENST00000613319.4:c.938T>A	ENSP00000480522.1:p.Ile313Asn
NM_001253727.1:c.1412T>A	NP_001240656.1:p.Ile471Asn
NM_001253728.1:c.1232T>A	NP_001240657.1:p.Ile411Asn
NM_001253729.1:c.1187T>A	NP_001240658.1:p.Ile396Asn
NM_001253730.1:c.938T>A	NP_001240659.1:p.Ile313Asn
NM_001253732.1:c.935T>A	NP_001240661.1:p.Ile312Asn
NM_001253733.1:c.863T>A	NP_001240662.1:p.Ile288Asn
NM_021634.3:c.1331T>A	NP_067647.2:p.Ile444Asn
NR_045579.1:n.2211T>A
NR_045580.1:n.1647T>A
NR_045581.1:n.1618T>A
NR_045582.1:n.1555T>A
NR_045583.1:n.1534T>A
NR_045584.1:n.1647T>A
XM_011532174.1:c.1409T>A	XP_011530476.1:p.Ile470Asn
XM_011532175.1:c.1340T>A	XP_011530477.1:p.Ile447Asn
XM_011532176.1:c.1259T>A	XP_011530478.1:p.Ile420Asn
XM_011532177.1:c.1169T>A	XP_011530479.1:p.Ile390Asn
XM_011532178.1:c.1169T>A	XP_011530480.1:p.Ile390Asn
XM_011532179.1:c.1196+5793T>A	XP_011530481.1:n.1196+5793T>A
NM_001363776.1:c.1088T>A	NP_001350705.1:p.Ile363Asn
XM_011532176.2:c.1259T>A	XP_011530478.1:p.Ile420Asn
XM_011532179.2:c.1196+5793T>A	XP_011530481.1:n.1196+5793T>A
XM_017008517.1:c.1337T>A	XP_016864006.1:p.Ile446Asn
XM_017008518.2:c.1328T>A	XP_016864007.1:p.Ile443Asn
XM_017008519.1:c.1169T>A	XP_016864008.1:p.Ile390Asn
XM_017008520.1:c.1169T>A	XP_016864009.1:p.Ile390Asn
XM_017008522.1:c.1085T>A	XP_016864011.1:p.Ile362Asn
XM_017008523.2:c.1115+5793T>A	XP_016864012.1:n.1115+5793T>A
XM_017008524.2:c.1043+5793T>A	XP_016864013.1:n.1043+5793T>A
XM_017008525.1:c.1016+5793T>A	XP_016864014.1:n.1016+5793T>A
XM_017008526.1:c.863T>A	XP_016864015.1:p.Ile288Asn
NM_021634.4:c.1331T>A MANE Select	NP_067647.2:p.Ile444Asn
NM_001253728.2:c.1232T>A	NP_001240657.1:p.Ile411Asn
NM_001253729.2:c.1187T>A	NP_001240658.1:p.Ile396Asn
NM_001253732.2:c.935T>A	NP_001240661.1:p.Ile312Asn
NR_045579.2:n.2043T>A
NR_045580.2:n.1479T>A
NR_045581.2:n.1450T>A
NR_045582.2:n.1387T>A
NR_045583.2:n.1366T>A
NR_045584.2:n.1479T>A
NM_001253727.2:c.1412T>A	NP_001240656.1:p.Ile471Asn
NM_001253730.2:c.938T>A	NP_001240659.1:p.Ile313Asn
NM_001253733.2:c.863T>A	NP_001240662.1:p.Ile288Asn