Canonical Allele Identifier: CA442140364

Gene: RXFP1

Linked Data

• MyVariant Identifiers: chr4:g.159566259G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.158645107G>A , CM000666.2:g.158645107G>A	GRCh38
NC_000004.11:g.159566259G>A , CM000666.1:g.159566259G>A	GRCh37
NC_000004.10:g.159785709G>A	NCBI36
NG_031835.1:g.128394G>A
NG_031835.2:g.128394G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307765.10:c.1314G>A MANE Select	ENSP00000303248.5:p.Lys438=
ENST00000307765.9:c.1314G>A	ENSP00000303248.5:p.Lys438=
ENST00000342048.9:c.*924G>A	ENSP00000432036.1:n.*924G>A
ENST00000343542.9:c.1170G>A	ENSP00000345889.5:p.Lys390=
ENST00000423548.5:c.1395G>A	ENSP00000405841.2:p.Lys465=
ENST00000448688.6:c.846G>A	ENSP00000414885.3:p.Lys282=
ENST00000460056.6:c.1071G>A	ENSP00000423306.1:p.Lys357=
ENST00000470033.2:c.1215G>A	ENSP00000420712.1:p.Lys405=
ENST00000471616.5:c.1367G>A	ENSP00000434475.1:n.1367G>A
ENST00000613319.4:c.921G>A	ENSP00000480522.1:p.Lys307=
NM_001253727.1:c.1395G>A	NP_001240656.1:p.Lys465=
NM_001253728.1:c.1215G>A	NP_001240657.1:p.Lys405=
NM_001253729.1:c.1170G>A	NP_001240658.1:p.Lys390=
NM_001253730.1:c.921G>A	NP_001240659.1:p.Lys307=
NM_001253732.1:c.918G>A	NP_001240661.1:p.Lys306=
NM_001253733.1:c.846G>A	NP_001240662.1:p.Lys282=
NM_021634.3:c.1314G>A	NP_067647.2:p.Lys438=
NR_045579.1:n.2194G>A
NR_045580.1:n.1630G>A
NR_045581.1:n.1601G>A
NR_045582.1:n.1538G>A
NR_045583.1:n.1517G>A
NR_045584.1:n.1630G>A
XM_011532174.1:c.1392G>A	XP_011530476.1:p.Lys464=
XM_011532175.1:c.1323G>A	XP_011530477.1:p.Lys441=
XM_011532176.1:c.1242G>A	XP_011530478.1:p.Lys414=
XM_011532177.1:c.1152G>A	XP_011530479.1:p.Lys384=
XM_011532178.1:c.1152G>A	XP_011530480.1:p.Lys384=
XM_011532179.1:c.1196+5776G>A	XP_011530481.1:n.1196+5776G>A
NM_001363776.1:c.1071G>A	NP_001350705.1:p.Lys357=
XM_011532176.2:c.1242G>A	XP_011530478.1:p.Lys414=
XM_011532179.2:c.1196+5776G>A	XP_011530481.1:n.1196+5776G>A
XM_017008517.1:c.1320G>A	XP_016864006.1:p.Lys440=
XM_017008518.2:c.1311G>A	XP_016864007.1:p.Lys437=
XM_017008519.1:c.1152G>A	XP_016864008.1:p.Lys384=
XM_017008520.1:c.1152G>A	XP_016864009.1:p.Lys384=
XM_017008522.1:c.1068G>A	XP_016864011.1:p.Lys356=
XM_017008523.2:c.1115+5776G>A	XP_016864012.1:n.1115+5776G>A
XM_017008524.2:c.1043+5776G>A	XP_016864013.1:n.1043+5776G>A
XM_017008525.1:c.1016+5776G>A	XP_016864014.1:n.1016+5776G>A
XM_017008526.1:c.846G>A	XP_016864015.1:p.Lys282=
NM_021634.4:c.1314G>A MANE Select	NP_067647.2:p.Lys438=
NM_001253728.2:c.1215G>A	NP_001240657.1:p.Lys405=
NM_001253729.2:c.1170G>A	NP_001240658.1:p.Lys390=
NM_001253732.2:c.918G>A	NP_001240661.1:p.Lys306=
NR_045579.2:n.2026G>A
NR_045580.2:n.1462G>A
NR_045581.2:n.1433G>A
NR_045582.2:n.1370G>A
NR_045583.2:n.1349G>A
NR_045584.2:n.1462G>A
NM_001253727.2:c.1395G>A	NP_001240656.1:p.Lys465=
NM_001253730.2:c.921G>A	NP_001240659.1:p.Lys307=
NM_001253733.2:c.846G>A	NP_001240662.1:p.Lys282=