Canonical Allele Identifier: CA358564125

Gene: RXFP1

Linked Data

• MyVariant Identifiers: chr4:g.159566252A>T (hg19) ; chr4:g.158645100A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.158645100A>T , CM000666.2:g.158645100A>T	GRCh38
NC_000004.11:g.159566252A>T , CM000666.1:g.159566252A>T	GRCh37
NC_000004.10:g.159785702A>T	NCBI36
NG_031835.1:g.128387A>T
NG_031835.2:g.128387A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307765.10:c.1307A>T MANE Select	ENSP00000303248.5:p.Glu436Val
ENST00000307765.9:c.1307A>T	ENSP00000303248.5:p.Glu436Val
ENST00000342048.9:c.*917A>T	ENSP00000432036.1:n.*917A>T
ENST00000343542.9:c.1163A>T	ENSP00000345889.5:p.Glu388Val
ENST00000423548.5:c.1388A>T	ENSP00000405841.2:p.Glu463Val
ENST00000448688.6:c.839A>T	ENSP00000414885.3:p.Glu280Val
ENST00000460056.6:c.1064A>T	ENSP00000423306.1:p.Glu355Val
ENST00000470033.2:c.1208A>T	ENSP00000420712.1:p.Glu403Val
ENST00000471616.5:c.1360A>T	ENSP00000434475.1:n.1360A>T
ENST00000613319.4:c.914A>T	ENSP00000480522.1:p.Glu305Val
NM_001253727.1:c.1388A>T	NP_001240656.1:p.Glu463Val
NM_001253728.1:c.1208A>T	NP_001240657.1:p.Glu403Val
NM_001253729.1:c.1163A>T	NP_001240658.1:p.Glu388Val
NM_001253730.1:c.914A>T	NP_001240659.1:p.Glu305Val
NM_001253732.1:c.911A>T	NP_001240661.1:p.Glu304Val
NM_001253733.1:c.839A>T	NP_001240662.1:p.Glu280Val
NM_021634.3:c.1307A>T	NP_067647.2:p.Glu436Val
NR_045579.1:n.2187A>T
NR_045580.1:n.1623A>T
NR_045581.1:n.1594A>T
NR_045582.1:n.1531A>T
NR_045583.1:n.1510A>T
NR_045584.1:n.1623A>T
XM_011532174.1:c.1385A>T	XP_011530476.1:p.Glu462Val
XM_011532175.1:c.1316A>T	XP_011530477.1:p.Glu439Val
XM_011532176.1:c.1235A>T	XP_011530478.1:p.Glu412Val
XM_011532177.1:c.1145A>T	XP_011530479.1:p.Glu382Val
XM_011532178.1:c.1145A>T	XP_011530480.1:p.Glu382Val
XM_011532179.1:c.1196+5769A>T	XP_011530481.1:n.1196+5769A>T
NM_001363776.1:c.1064A>T	NP_001350705.1:p.Glu355Val
XM_011532176.2:c.1235A>T	XP_011530478.1:p.Glu412Val
XM_011532179.2:c.1196+5769A>T	XP_011530481.1:n.1196+5769A>T
XM_017008517.1:c.1313A>T	XP_016864006.1:p.Glu438Val
XM_017008518.2:c.1304A>T	XP_016864007.1:p.Glu435Val
XM_017008519.1:c.1145A>T	XP_016864008.1:p.Glu382Val
XM_017008520.1:c.1145A>T	XP_016864009.1:p.Glu382Val
XM_017008522.1:c.1061A>T	XP_016864011.1:p.Glu354Val
XM_017008523.2:c.1115+5769A>T	XP_016864012.1:n.1115+5769A>T
XM_017008524.2:c.1043+5769A>T	XP_016864013.1:n.1043+5769A>T
XM_017008525.1:c.1016+5769A>T	XP_016864014.1:n.1016+5769A>T
XM_017008526.1:c.839A>T	XP_016864015.1:p.Glu280Val
NM_021634.4:c.1307A>T MANE Select	NP_067647.2:p.Glu436Val
NM_001253728.2:c.1208A>T	NP_001240657.1:p.Glu403Val
NM_001253729.2:c.1163A>T	NP_001240658.1:p.Glu388Val
NM_001253732.2:c.911A>T	NP_001240661.1:p.Glu304Val
NR_045579.2:n.2019A>T
NR_045580.2:n.1455A>T
NR_045581.2:n.1426A>T
NR_045582.2:n.1363A>T
NR_045583.2:n.1342A>T
NR_045584.2:n.1455A>T
NM_001253727.2:c.1388A>T	NP_001240656.1:p.Glu463Val
NM_001253730.2:c.914A>T	NP_001240659.1:p.Glu305Val
NM_001253733.2:c.839A>T	NP_001240662.1:p.Glu280Val