Canonical Allele Identifier: CA358564135

Gene: RXFP1

Linked Data

• MyVariant Identifiers: chr4:g.159566255A>T (hg19) ; chr4:g.158645103A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.158645103A>T , CM000666.2:g.158645103A>T	GRCh38
NC_000004.11:g.159566255A>T , CM000666.1:g.159566255A>T	GRCh37
NC_000004.10:g.159785705A>T	NCBI36
NG_031835.1:g.128390A>T
NG_031835.2:g.128390A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307765.10:c.1310A>T MANE Select	ENSP00000303248.5:p.Asn437Ile
ENST00000307765.9:c.1310A>T	ENSP00000303248.5:p.Asn437Ile
ENST00000342048.9:c.*920A>T	ENSP00000432036.1:n.*920A>T
ENST00000343542.9:c.1166A>T	ENSP00000345889.5:p.Asn389Ile
ENST00000423548.5:c.1391A>T	ENSP00000405841.2:p.Asn464Ile
ENST00000448688.6:c.842A>T	ENSP00000414885.3:p.Asn281Ile
ENST00000460056.6:c.1067A>T	ENSP00000423306.1:p.Asn356Ile
ENST00000470033.2:c.1211A>T	ENSP00000420712.1:p.Asn404Ile
ENST00000471616.5:c.1363A>T	ENSP00000434475.1:n.1363A>T
ENST00000613319.4:c.917A>T	ENSP00000480522.1:p.Asn306Ile
NM_001253727.1:c.1391A>T	NP_001240656.1:p.Asn464Ile
NM_001253728.1:c.1211A>T	NP_001240657.1:p.Asn404Ile
NM_001253729.1:c.1166A>T	NP_001240658.1:p.Asn389Ile
NM_001253730.1:c.917A>T	NP_001240659.1:p.Asn306Ile
NM_001253732.1:c.914A>T	NP_001240661.1:p.Asn305Ile
NM_001253733.1:c.842A>T	NP_001240662.1:p.Asn281Ile
NM_021634.3:c.1310A>T	NP_067647.2:p.Asn437Ile
NR_045579.1:n.2190A>T
NR_045580.1:n.1626A>T
NR_045581.1:n.1597A>T
NR_045582.1:n.1534A>T
NR_045583.1:n.1513A>T
NR_045584.1:n.1626A>T
XM_011532174.1:c.1388A>T	XP_011530476.1:p.Asn463Ile
XM_011532175.1:c.1319A>T	XP_011530477.1:p.Asn440Ile
XM_011532176.1:c.1238A>T	XP_011530478.1:p.Asn413Ile
XM_011532177.1:c.1148A>T	XP_011530479.1:p.Asn383Ile
XM_011532178.1:c.1148A>T	XP_011530480.1:p.Asn383Ile
XM_011532179.1:c.1196+5772A>T	XP_011530481.1:n.1196+5772A>T
NM_001363776.1:c.1067A>T	NP_001350705.1:p.Asn356Ile
XM_011532176.2:c.1238A>T	XP_011530478.1:p.Asn413Ile
XM_011532179.2:c.1196+5772A>T	XP_011530481.1:n.1196+5772A>T
XM_017008517.1:c.1316A>T	XP_016864006.1:p.Asn439Ile
XM_017008518.2:c.1307A>T	XP_016864007.1:p.Asn436Ile
XM_017008519.1:c.1148A>T	XP_016864008.1:p.Asn383Ile
XM_017008520.1:c.1148A>T	XP_016864009.1:p.Asn383Ile
XM_017008522.1:c.1064A>T	XP_016864011.1:p.Asn355Ile
XM_017008523.2:c.1115+5772A>T	XP_016864012.1:n.1115+5772A>T
XM_017008524.2:c.1043+5772A>T	XP_016864013.1:n.1043+5772A>T
XM_017008525.1:c.1016+5772A>T	XP_016864014.1:n.1016+5772A>T
XM_017008526.1:c.842A>T	XP_016864015.1:p.Asn281Ile
NM_021634.4:c.1310A>T MANE Select	NP_067647.2:p.Asn437Ile
NM_001253728.2:c.1211A>T	NP_001240657.1:p.Asn404Ile
NM_001253729.2:c.1166A>T	NP_001240658.1:p.Asn389Ile
NM_001253732.2:c.914A>T	NP_001240661.1:p.Asn305Ile
NR_045579.2:n.2022A>T
NR_045580.2:n.1458A>T
NR_045581.2:n.1429A>T
NR_045582.2:n.1366A>T
NR_045583.2:n.1345A>T
NR_045584.2:n.1458A>T
NM_001253727.2:c.1391A>T	NP_001240656.1:p.Asn464Ile
NM_001253730.2:c.917A>T	NP_001240659.1:p.Asn306Ile
NM_001253733.2:c.842A>T	NP_001240662.1:p.Asn281Ile