Canonical Allele Identifier: CA358564146

Gene: RXFP1

Linked Data

• MyVariant Identifiers: chr4:g.159566260C>A (hg19) ; chr4:g.158645108C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.158645108C>A , CM000666.2:g.158645108C>A	GRCh38
NC_000004.11:g.159566260C>A , CM000666.1:g.159566260C>A	GRCh37
NC_000004.10:g.159785710C>A	NCBI36
NG_031835.1:g.128395C>A
NG_031835.2:g.128395C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307765.10:c.1315C>A MANE Select	ENSP00000303248.5:p.Leu439Met
ENST00000307765.9:c.1315C>A	ENSP00000303248.5:p.Leu439Met
ENST00000342048.9:c.*925C>A	ENSP00000432036.1:n.*925C>A
ENST00000343542.9:c.1171C>A	ENSP00000345889.5:p.Leu391Met
ENST00000423548.5:c.1396C>A	ENSP00000405841.2:p.Leu466Met
ENST00000448688.6:c.847C>A	ENSP00000414885.3:p.Leu283Met
ENST00000460056.6:c.1072C>A	ENSP00000423306.1:p.Leu358Met
ENST00000470033.2:c.1216C>A	ENSP00000420712.1:p.Leu406Met
ENST00000471616.5:c.1368C>A	ENSP00000434475.1:n.1368C>A
ENST00000613319.4:c.922C>A	ENSP00000480522.1:p.Leu308Met
NM_001253727.1:c.1396C>A	NP_001240656.1:p.Leu466Met
NM_001253728.1:c.1216C>A	NP_001240657.1:p.Leu406Met
NM_001253729.1:c.1171C>A	NP_001240658.1:p.Leu391Met
NM_001253730.1:c.922C>A	NP_001240659.1:p.Leu308Met
NM_001253732.1:c.919C>A	NP_001240661.1:p.Leu307Met
NM_001253733.1:c.847C>A	NP_001240662.1:p.Leu283Met
NM_021634.3:c.1315C>A	NP_067647.2:p.Leu439Met
NR_045579.1:n.2195C>A
NR_045580.1:n.1631C>A
NR_045581.1:n.1602C>A
NR_045582.1:n.1539C>A
NR_045583.1:n.1518C>A
NR_045584.1:n.1631C>A
XM_011532174.1:c.1393C>A	XP_011530476.1:p.Leu465Met
XM_011532175.1:c.1324C>A	XP_011530477.1:p.Leu442Met
XM_011532176.1:c.1243C>A	XP_011530478.1:p.Leu415Met
XM_011532177.1:c.1153C>A	XP_011530479.1:p.Leu385Met
XM_011532178.1:c.1153C>A	XP_011530480.1:p.Leu385Met
XM_011532179.1:c.1196+5777C>A	XP_011530481.1:n.1196+5777C>A
NM_001363776.1:c.1072C>A	NP_001350705.1:p.Leu358Met
XM_011532176.2:c.1243C>A	XP_011530478.1:p.Leu415Met
XM_011532179.2:c.1196+5777C>A	XP_011530481.1:n.1196+5777C>A
XM_017008517.1:c.1321C>A	XP_016864006.1:p.Leu441Met
XM_017008518.2:c.1312C>A	XP_016864007.1:p.Leu438Met
XM_017008519.1:c.1153C>A	XP_016864008.1:p.Leu385Met
XM_017008520.1:c.1153C>A	XP_016864009.1:p.Leu385Met
XM_017008522.1:c.1069C>A	XP_016864011.1:p.Leu357Met
XM_017008523.2:c.1115+5777C>A	XP_016864012.1:n.1115+5777C>A
XM_017008524.2:c.1043+5777C>A	XP_016864013.1:n.1043+5777C>A
XM_017008525.1:c.1016+5777C>A	XP_016864014.1:n.1016+5777C>A
XM_017008526.1:c.847C>A	XP_016864015.1:p.Leu283Met
NM_021634.4:c.1315C>A MANE Select	NP_067647.2:p.Leu439Met
NM_001253728.2:c.1216C>A	NP_001240657.1:p.Leu406Met
NM_001253729.2:c.1171C>A	NP_001240658.1:p.Leu391Met
NM_001253732.2:c.919C>A	NP_001240661.1:p.Leu307Met
NR_045579.2:n.2027C>A
NR_045580.2:n.1463C>A
NR_045581.2:n.1434C>A
NR_045582.2:n.1371C>A
NR_045583.2:n.1350C>A
NR_045584.2:n.1463C>A
NM_001253727.2:c.1396C>A	NP_001240656.1:p.Leu466Met
NM_001253730.2:c.922C>A	NP_001240659.1:p.Leu308Met
NM_001253733.2:c.847C>A	NP_001240662.1:p.Leu283Met