Canonical Allele Identifier: CA442140379

Gene: RXFP1

Linked Data

• MyVariant Identifiers: chr4:g.159566268C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.158645116C>T , CM000666.2:g.158645116C>T	GRCh38
NC_000004.11:g.159566268C>T , CM000666.1:g.159566268C>T	GRCh37
NC_000004.10:g.159785718C>T	NCBI36
NG_031835.1:g.128403C>T
NG_031835.2:g.128403C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307765.10:c.1323C>T MANE Select	ENSP00000303248.5:p.Ala441=
ENST00000307765.9:c.1323C>T	ENSP00000303248.5:p.Ala441=
ENST00000342048.9:c.*933C>T	ENSP00000432036.1:n.*933C>T
ENST00000343542.9:c.1179C>T	ENSP00000345889.5:p.Ala393=
ENST00000423548.5:c.1404C>T	ENSP00000405841.2:p.Ala468=
ENST00000448688.6:c.855C>T	ENSP00000414885.3:p.Ala285=
ENST00000460056.6:c.1080C>T	ENSP00000423306.1:p.Ala360=
ENST00000470033.2:c.1224C>T	ENSP00000420712.1:p.Ala408=
ENST00000471616.5:c.1376C>T	ENSP00000434475.1:n.1376C>T
ENST00000613319.4:c.930C>T	ENSP00000480522.1:p.Ala310=
NM_001253727.1:c.1404C>T	NP_001240656.1:p.Ala468=
NM_001253728.1:c.1224C>T	NP_001240657.1:p.Ala408=
NM_001253729.1:c.1179C>T	NP_001240658.1:p.Ala393=
NM_001253730.1:c.930C>T	NP_001240659.1:p.Ala310=
NM_001253732.1:c.927C>T	NP_001240661.1:p.Ala309=
NM_001253733.1:c.855C>T	NP_001240662.1:p.Ala285=
NM_021634.3:c.1323C>T	NP_067647.2:p.Ala441=
NR_045579.1:n.2203C>T
NR_045580.1:n.1639C>T
NR_045581.1:n.1610C>T
NR_045582.1:n.1547C>T
NR_045583.1:n.1526C>T
NR_045584.1:n.1639C>T
XM_011532174.1:c.1401C>T	XP_011530476.1:p.Ala467=
XM_011532175.1:c.1332C>T	XP_011530477.1:p.Ala444=
XM_011532176.1:c.1251C>T	XP_011530478.1:p.Ala417=
XM_011532177.1:c.1161C>T	XP_011530479.1:p.Ala387=
XM_011532178.1:c.1161C>T	XP_011530480.1:p.Ala387=
XM_011532179.1:c.1196+5785C>T	XP_011530481.1:n.1196+5785C>T
NM_001363776.1:c.1080C>T	NP_001350705.1:p.Ala360=
XM_011532176.2:c.1251C>T	XP_011530478.1:p.Ala417=
XM_011532179.2:c.1196+5785C>T	XP_011530481.1:n.1196+5785C>T
XM_017008517.1:c.1329C>T	XP_016864006.1:p.Ala443=
XM_017008518.2:c.1320C>T	XP_016864007.1:p.Ala440=
XM_017008519.1:c.1161C>T	XP_016864008.1:p.Ala387=
XM_017008520.1:c.1161C>T	XP_016864009.1:p.Ala387=
XM_017008522.1:c.1077C>T	XP_016864011.1:p.Ala359=
XM_017008523.2:c.1115+5785C>T	XP_016864012.1:n.1115+5785C>T
XM_017008524.2:c.1043+5785C>T	XP_016864013.1:n.1043+5785C>T
XM_017008525.1:c.1016+5785C>T	XP_016864014.1:n.1016+5785C>T
XM_017008526.1:c.855C>T	XP_016864015.1:p.Ala285=
NM_021634.4:c.1323C>T MANE Select	NP_067647.2:p.Ala441=
NM_001253728.2:c.1224C>T	NP_001240657.1:p.Ala408=
NM_001253729.2:c.1179C>T	NP_001240658.1:p.Ala393=
NM_001253732.2:c.927C>T	NP_001240661.1:p.Ala309=
NR_045579.2:n.2035C>T
NR_045580.2:n.1471C>T
NR_045581.2:n.1442C>T
NR_045582.2:n.1379C>T
NR_045583.2:n.1358C>T
NR_045584.2:n.1471C>T
NM_001253727.2:c.1404C>T	NP_001240656.1:p.Ala468=
NM_001253730.2:c.930C>T	NP_001240659.1:p.Ala310=
NM_001253733.2:c.855C>T	NP_001240662.1:p.Ala285=