Canonical Allele Identifier: CA1562918434

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823795T= , CM000667.2:g.90823795T=	GRCh38
NC_000005.9:g.90119612T= , CM000667.1:g.90119612T=	GRCh37
NC_000005.8:g.90155368T=	NCBI36
NG_007083.1:g.269996T=
NG_007083.2:g.299452T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16368+199T= MANE Select	ENSP00000384582.2:n.16368+199T=
ENST00000425867.3:c.5322+199T=	ENSP00000392618.3:n.5322+199T=
ENST00000638510.1:n.3635+199T=
ENST00000639431.1:c.265+147586T=	ENSP00000491057.1:n.265+147586T=
ENST00000640061.1:n.128+1613T=
ENST00000640407.1:c.2778+199T=	ENSP00000491425.1:n.2778+199T=
ENST00000405460.6:c.16368+199T=	ENSP00000384582.2:n.16368+199T=
ENST00000425867.2:c.3351+199T=	ENSP00000392618.2:n.3351+199T=
NM_032119.3:c.16368+199T=	NP_115495.3:n.16368+199T=
NR_003149.1:n.16381+199T=
XM_011543675.1:c.16365+199T=	XP_011541977.1:n.16365+199T=
XM_011543676.1:c.16287+199T=	XP_011541978.1:n.16287+199T=
XM_011543677.1:c.13671+199T=	XP_011541979.1:n.13671+199T=
NM_032119.4:c.16368+199T= MANE Select	NP_115495.3:n.16368+199T=
XM_017009963.2:c.16389+199T=	XP_016865452.1:n.16389+199T=
XM_017009964.2:c.16386+199T=	XP_016865453.1:n.16386+199T=
XM_017009965.1:c.16386+199T=	XP_016865454.1:n.16386+199T=
XM_017009966.2:c.16308+199T=	XP_016865455.1:n.16308+199T=
XM_017009967.1:c.16293+199T=	XP_016865456.1:n.16293+199T=
XM_017009968.2:c.16209+199T=	XP_016865457.1:n.16209+199T=
XM_017009969.2:c.16389+199T=	XP_016865458.1:n.16389+199T=
XM_017009972.1:c.9507+199T=	XP_016865461.1:n.9507+199T=
XM_017009973.1:c.9486+199T=	XP_016865462.1:n.9486+199T=
NR_003149.2:n.16384+199T=