Canonical Allele Identifier: CA1562867551

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712384T= , CM000667.2:g.90712384T=	GRCh38
NC_000005.9:g.90008201T= , CM000667.1:g.90008201T=	GRCh37
NC_000005.8:g.90043957T=	NCBI36
NG_007083.1:g.158585T=
NG_007083.2:g.188041T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9140T= MANE Select	ENSP00000384582.2:p.Leu3047=
ENST00000639431.1:c.265+36175T=	ENSP00000491057.1:n.265+36175T=
ENST00000639473.1:n.4599T=
ENST00000640012.1:c.2947T=
ENST00000640374.1:n.2284T=
ENST00000640779.1:c.3869T=
ENST00000405460.6:c.9140T=	ENSP00000384582.2:p.Leu3047=
ENST00000509621.1:c.1837T=
NM_032119.3:c.9140T=	NP_115495.3:p.Leu3047=
NR_003149.1:n.9153T=
XM_011543675.1:c.9137T=	XP_011541977.1:p.Leu3046=
XM_011543676.1:c.9059T=	XP_011541978.1:p.Leu3020=
XM_011543677.1:c.6443T=	XP_011541979.1:p.Leu2148=
XM_011543678.1:c.9140T=	XP_011541980.1:p.Leu3047=
XM_011543679.1:c.9140T=	XP_011541981.1:p.Leu3047=
XR_948560.1:n.462A=
NM_032119.4:c.9140T= MANE Select	NP_115495.3:p.Leu3047=
XM_017009963.2:c.9161T=	XP_016865452.1:p.Leu3054=
XM_017009964.2:c.9158T=	XP_016865453.1:p.Leu3053=
XM_017009965.1:c.9158T=	XP_016865454.1:p.Leu3053=
XM_017009966.2:c.9080T=	XP_016865455.1:p.Leu3027=
XM_017009967.1:c.9065T=	XP_016865456.1:p.Leu3022=
XM_017009968.2:c.9161T=	XP_016865457.1:p.Leu3054=
XM_017009969.2:c.9161T=	XP_016865458.1:p.Leu3054=
XM_017009970.2:c.9161T=	XP_016865459.1:p.Leu3054=
XM_017009971.2:c.9161T=	XP_016865460.1:p.Leu3054=
XM_017009972.1:c.2279T=	XP_016865461.1:p.Leu760=
XM_017009973.1:c.2258T=	XP_016865462.1:p.Leu753=
XM_017009974.2:c.9161T=	XP_016865463.1:p.Leu3054=
NR_003149.2:n.9156T=