Canonical Allele Identifier: CA358564129

Gene: RXFP1

Linked Data

• MyVariant Identifiers: chr4:g.159566253G>T (hg19) ; chr4:g.158645101G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.158645101G>T , CM000666.2:g.158645101G>T	GRCh38
NC_000004.11:g.159566253G>T , CM000666.1:g.159566253G>T	GRCh37
NC_000004.10:g.159785703G>T	NCBI36
NG_031835.1:g.128388G>T
NG_031835.2:g.128388G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307765.10:c.1308G>T MANE Select	ENSP00000303248.5:p.Glu436Asp
ENST00000307765.9:c.1308G>T	ENSP00000303248.5:p.Glu436Asp
ENST00000342048.9:c.*918G>T	ENSP00000432036.1:n.*918G>T
ENST00000343542.9:c.1164G>T	ENSP00000345889.5:p.Glu388Asp
ENST00000423548.5:c.1389G>T	ENSP00000405841.2:p.Glu463Asp
ENST00000448688.6:c.840G>T	ENSP00000414885.3:p.Glu280Asp
ENST00000460056.6:c.1065G>T	ENSP00000423306.1:p.Glu355Asp
ENST00000470033.2:c.1209G>T	ENSP00000420712.1:p.Glu403Asp
ENST00000471616.5:c.1361G>T	ENSP00000434475.1:n.1361G>T
ENST00000613319.4:c.915G>T	ENSP00000480522.1:p.Glu305Asp
NM_001253727.1:c.1389G>T	NP_001240656.1:p.Glu463Asp
NM_001253728.1:c.1209G>T	NP_001240657.1:p.Glu403Asp
NM_001253729.1:c.1164G>T	NP_001240658.1:p.Glu388Asp
NM_001253730.1:c.915G>T	NP_001240659.1:p.Glu305Asp
NM_001253732.1:c.912G>T	NP_001240661.1:p.Glu304Asp
NM_001253733.1:c.840G>T	NP_001240662.1:p.Glu280Asp
NM_021634.3:c.1308G>T	NP_067647.2:p.Glu436Asp
NR_045579.1:n.2188G>T
NR_045580.1:n.1624G>T
NR_045581.1:n.1595G>T
NR_045582.1:n.1532G>T
NR_045583.1:n.1511G>T
NR_045584.1:n.1624G>T
XM_011532174.1:c.1386G>T	XP_011530476.1:p.Glu462Asp
XM_011532175.1:c.1317G>T	XP_011530477.1:p.Glu439Asp
XM_011532176.1:c.1236G>T	XP_011530478.1:p.Glu412Asp
XM_011532177.1:c.1146G>T	XP_011530479.1:p.Glu382Asp
XM_011532178.1:c.1146G>T	XP_011530480.1:p.Glu382Asp
XM_011532179.1:c.1196+5770G>T	XP_011530481.1:n.1196+5770G>T
NM_001363776.1:c.1065G>T	NP_001350705.1:p.Glu355Asp
XM_011532176.2:c.1236G>T	XP_011530478.1:p.Glu412Asp
XM_011532179.2:c.1196+5770G>T	XP_011530481.1:n.1196+5770G>T
XM_017008517.1:c.1314G>T	XP_016864006.1:p.Glu438Asp
XM_017008518.2:c.1305G>T	XP_016864007.1:p.Glu435Asp
XM_017008519.1:c.1146G>T	XP_016864008.1:p.Glu382Asp
XM_017008520.1:c.1146G>T	XP_016864009.1:p.Glu382Asp
XM_017008522.1:c.1062G>T	XP_016864011.1:p.Glu354Asp
XM_017008523.2:c.1115+5770G>T	XP_016864012.1:n.1115+5770G>T
XM_017008524.2:c.1043+5770G>T	XP_016864013.1:n.1043+5770G>T
XM_017008525.1:c.1016+5770G>T	XP_016864014.1:n.1016+5770G>T
XM_017008526.1:c.840G>T	XP_016864015.1:p.Glu280Asp
NM_021634.4:c.1308G>T MANE Select	NP_067647.2:p.Glu436Asp
NM_001253728.2:c.1209G>T	NP_001240657.1:p.Glu403Asp
NM_001253729.2:c.1164G>T	NP_001240658.1:p.Glu388Asp
NM_001253732.2:c.912G>T	NP_001240661.1:p.Glu304Asp
NR_045579.2:n.2020G>T
NR_045580.2:n.1456G>T
NR_045581.2:n.1427G>T
NR_045582.2:n.1364G>T
NR_045583.2:n.1343G>T
NR_045584.2:n.1456G>T
NM_001253727.2:c.1389G>T	NP_001240656.1:p.Glu463Asp
NM_001253730.2:c.915G>T	NP_001240659.1:p.Glu305Asp
NM_001253733.2:c.840G>T	NP_001240662.1:p.Glu280Asp