Canonical Allele Identifier: CA1562829316

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90627293T= , CM000667.2:g.90627293T=	GRCh38
NC_000005.9:g.89923110T= , CM000667.1:g.89923110T=	GRCh37
NC_000005.8:g.89958866T=	NCBI36
NG_007083.1:g.73494T=
NG_007083.2:g.102950T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.755T= MANE Select	ENSP00000384582.2:p.Ile252=
ENST00000640083.1:n.460T=
ENST00000640109.1:n.851T=
ENST00000640281.1:n.814T=
ENST00000405460.6:c.755T=	ENSP00000384582.2:p.Ile252=
NM_032119.3:c.755T=	NP_115495.3:p.Ile252=
NR_003149.1:n.851T=
XM_011543675.1:c.755T=	XP_011541977.1:p.Ile252=
XM_011543676.1:c.755T=	XP_011541978.1:p.Ile252=
XM_011543678.1:c.755T=	XP_011541980.1:p.Ile252=
XM_011543679.1:c.755T=	XP_011541981.1:p.Ile252=
NM_032119.4:c.755T= MANE Select	NP_115495.3:p.Ile252=
XM_017009963.2:c.755T=	XP_016865452.1:p.Ile252=
XM_017009964.2:c.755T=	XP_016865453.1:p.Ile252=
XM_017009965.1:c.752T=	XP_016865454.1:p.Ile251=
XM_017009966.2:c.755T=	XP_016865455.1:p.Ile252=
XM_017009967.1:c.659T=	XP_016865456.1:p.Ile220=
XM_017009968.2:c.755T=	XP_016865457.1:p.Ile252=
XM_017009969.2:c.755T=	XP_016865458.1:p.Ile252=
XM_017009970.2:c.755T=	XP_016865459.1:p.Ile252=
XM_017009971.2:c.755T=	XP_016865460.1:p.Ile252=
XM_017009974.2:c.755T=	XP_016865463.1:p.Ile252=
NR_003149.2:n.854T=