Canonical Allele Identifier: CA442140361

Gene: RXFP1

Linked Data

• dbSNP Id: rs1306398408
• MyVariant Identifiers: chr4:g.159566256C>T (hg19) ; chr4:g.158645104C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.158645104C>T , CM000666.2:g.158645104C>T	GRCh38
NC_000004.11:g.159566256C>T , CM000666.1:g.159566256C>T	GRCh37
NC_000004.10:g.159785706C>T	NCBI36
NG_031835.1:g.128391C>T
NG_031835.2:g.128391C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307765.10:c.1311C>T MANE Select	ENSP00000303248.5:p.Asn437=
ENST00000307765.9:c.1311C>T	ENSP00000303248.5:p.Asn437=
ENST00000342048.9:c.*921C>T	ENSP00000432036.1:n.*921C>T
ENST00000343542.9:c.1167C>T	ENSP00000345889.5:p.Asn389=
ENST00000423548.5:c.1392C>T	ENSP00000405841.2:p.Asn464=
ENST00000448688.6:c.843C>T	ENSP00000414885.3:p.Asn281=
ENST00000460056.6:c.1068C>T	ENSP00000423306.1:p.Asn356=
ENST00000470033.2:c.1212C>T	ENSP00000420712.1:p.Asn404=
ENST00000471616.5:c.1364C>T	ENSP00000434475.1:n.1364C>T
ENST00000613319.4:c.918C>T	ENSP00000480522.1:p.Asn306=
NM_001253727.1:c.1392C>T	NP_001240656.1:p.Asn464=
NM_001253728.1:c.1212C>T	NP_001240657.1:p.Asn404=
NM_001253729.1:c.1167C>T	NP_001240658.1:p.Asn389=
NM_001253730.1:c.918C>T	NP_001240659.1:p.Asn306=
NM_001253732.1:c.915C>T	NP_001240661.1:p.Asn305=
NM_001253733.1:c.843C>T	NP_001240662.1:p.Asn281=
NM_021634.3:c.1311C>T	NP_067647.2:p.Asn437=
NR_045579.1:n.2191C>T
NR_045580.1:n.1627C>T
NR_045581.1:n.1598C>T
NR_045582.1:n.1535C>T
NR_045583.1:n.1514C>T
NR_045584.1:n.1627C>T
XM_011532174.1:c.1389C>T	XP_011530476.1:p.Asn463=
XM_011532175.1:c.1320C>T	XP_011530477.1:p.Asn440=
XM_011532176.1:c.1239C>T	XP_011530478.1:p.Asn413=
XM_011532177.1:c.1149C>T	XP_011530479.1:p.Asn383=
XM_011532178.1:c.1149C>T	XP_011530480.1:p.Asn383=
XM_011532179.1:c.1196+5773C>T	XP_011530481.1:n.1196+5773C>T
NM_001363776.1:c.1068C>T	NP_001350705.1:p.Asn356=
XM_011532176.2:c.1239C>T	XP_011530478.1:p.Asn413=
XM_011532179.2:c.1196+5773C>T	XP_011530481.1:n.1196+5773C>T
XM_017008517.1:c.1317C>T	XP_016864006.1:p.Asn439=
XM_017008518.2:c.1308C>T	XP_016864007.1:p.Asn436=
XM_017008519.1:c.1149C>T	XP_016864008.1:p.Asn383=
XM_017008520.1:c.1149C>T	XP_016864009.1:p.Asn383=
XM_017008522.1:c.1065C>T	XP_016864011.1:p.Asn355=
XM_017008523.2:c.1115+5773C>T	XP_016864012.1:n.1115+5773C>T
XM_017008524.2:c.1043+5773C>T	XP_016864013.1:n.1043+5773C>T
XM_017008525.1:c.1016+5773C>T	XP_016864014.1:n.1016+5773C>T
XM_017008526.1:c.843C>T	XP_016864015.1:p.Asn281=
NM_021634.4:c.1311C>T MANE Select	NP_067647.2:p.Asn437=
NM_001253728.2:c.1212C>T	NP_001240657.1:p.Asn404=
NM_001253729.2:c.1167C>T	NP_001240658.1:p.Asn389=
NM_001253732.2:c.915C>T	NP_001240661.1:p.Asn305=
NR_045579.2:n.2023C>T
NR_045580.2:n.1459C>T
NR_045581.2:n.1430C>T
NR_045582.2:n.1367C>T
NR_045583.2:n.1346C>T
NR_045584.2:n.1459C>T
NM_001253727.2:c.1392C>T	NP_001240656.1:p.Asn464=
NM_001253730.2:c.918C>T	NP_001240659.1:p.Asn306=
NM_001253733.2:c.843C>T	NP_001240662.1:p.Asn281=