Canonical Allele Identifier: CA445414044

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90012534T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716717T>A , CM000667.2:g.90716717T>A	GRCh38
NC_000005.9:g.90012534T>A , CM000667.1:g.90012534T>A	GRCh37
NC_000005.8:g.90048290T>A	NCBI36
NG_007083.1:g.162918T>A
NG_007083.2:g.192374T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9435T>A MANE Select	ENSP00000384582.2:p.Gly3145=
ENST00000639431.1:c.265+40508T>A	ENSP00000491057.1:n.265+40508T>A
ENST00000639473.1:n.4894T>A
ENST00000640374.1:n.2579T>A
ENST00000640779.1:c.4164T>A
ENST00000405460.6:c.9435T>A	ENSP00000384582.2:p.Gly3145=
ENST00000509621.1:c.2132T>A
NM_032119.3:c.9435T>A	NP_115495.3:p.Gly3145=
NR_003149.1:n.9448T>A
XM_011543675.1:c.9432T>A	XP_011541977.1:p.Gly3144=
XM_011543676.1:c.9354T>A	XP_011541978.1:p.Gly3118=
XM_011543677.1:c.6738T>A	XP_011541979.1:p.Gly2246=
XM_011543678.1:c.9435T>A	XP_011541980.1:p.Gly3145=
XM_011543679.1:c.9435T>A	XP_011541981.1:p.Gly3145=
XR_948560.1:n.272-908A>T
NM_032119.4:c.9435T>A MANE Select	NP_115495.3:p.Gly3145=
XM_017009963.2:c.9456T>A	XP_016865452.1:p.Gly3152=
XM_017009964.2:c.9453T>A	XP_016865453.1:p.Gly3151=
XM_017009965.1:c.9453T>A	XP_016865454.1:p.Gly3151=
XM_017009966.2:c.9375T>A	XP_016865455.1:p.Gly3125=
XM_017009967.1:c.9360T>A	XP_016865456.1:p.Gly3120=
XM_017009968.2:c.9456T>A	XP_016865457.1:p.Gly3152=
XM_017009969.2:c.9456T>A	XP_016865458.1:p.Gly3152=
XM_017009970.2:c.9456T>A	XP_016865459.1:p.Gly3152=
XM_017009971.2:c.9456T>A	XP_016865460.1:p.Gly3152=
XM_017009972.1:c.2574T>A	XP_016865461.1:p.Gly858=
XM_017009973.1:c.2553T>A	XP_016865462.1:p.Gly851=
XM_017009974.2:c.9456T>A	XP_016865463.1:p.Gly3152=
XR_001742802.1:n.2523-908A>T
NR_003149.2:n.9451T>A