Canonical Allele Identifier: CA1562886202

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755094C= , CM000667.2:g.90755094C=	GRCh38
NC_000005.9:g.90050911C= , CM000667.1:g.90050911C=	GRCh37
NC_000005.8:g.90086667C=	NCBI36
NG_007083.1:g.201295C=
NG_007083.2:g.230751C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11489C= MANE Select	ENSP00000384582.2:p.Ala3830=
ENST00000425867.3:c.620C=	ENSP00000392618.3:p.Ala207=
ENST00000639431.1:c.265+78885C=	ENSP00000491057.1:n.265+78885C=
ENST00000640374.1:n.4633C=
ENST00000640464.1:n.1908C=
ENST00000405460.6:c.11489C=	ENSP00000384582.2:p.Ala3830=
ENST00000509621.1:c.4186C=
NM_032119.3:c.11489C=	NP_115495.3:p.Ala3830=
NR_003149.1:n.11502C=
XM_011543675.1:c.11486C=	XP_011541977.1:p.Ala3829=
XM_011543676.1:c.11408C=	XP_011541978.1:p.Ala3803=
XM_011543677.1:c.8792C=	XP_011541979.1:p.Ala2931=
XM_011543678.1:c.11489C=	XP_011541980.1:p.Ala3830=
NM_032119.4:c.11489C= MANE Select	NP_115495.3:p.Ala3830=
XM_017009963.2:c.11510C=	XP_016865452.1:p.Ala3837=
XM_017009964.2:c.11507C=	XP_016865453.1:p.Ala3836=
XM_017009965.1:c.11507C=	XP_016865454.1:p.Ala3836=
XM_017009966.2:c.11429C=	XP_016865455.1:p.Ala3810=
XM_017009967.1:c.11414C=	XP_016865456.1:p.Ala3805=
XM_017009968.2:c.11510C=	XP_016865457.1:p.Ala3837=
XM_017009969.2:c.11510C=	XP_016865458.1:p.Ala3837=
XM_017009970.2:c.11510C=	XP_016865459.1:p.Ala3837=
XM_017009971.2:c.11510C=	XP_016865460.1:p.Ala3837=
XM_017009972.1:c.4628C=	XP_016865461.1:p.Ala1543=
XM_017009973.1:c.4607C=	XP_016865462.1:p.Ala1536=
NR_003149.2:n.11505C=