Canonical Allele Identifier: CA445415722

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90040894T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745077T>A , CM000667.2:g.90745077T>A	GRCh38
NC_000005.9:g.90040894T>A , CM000667.1:g.90040894T>A	GRCh37
NC_000005.8:g.90076650T>A	NCBI36
NG_007083.1:g.191278T>A
NG_007083.2:g.220734T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.10581T>A MANE Select	ENSP00000384582.2:p.Ser3527=
ENST00000639431.1:c.265+68868T>A	ENSP00000491057.1:n.265+68868T>A
ENST00000640374.1:n.3725T>A
ENST00000640464.1:n.1000T>A
ENST00000405460.6:c.10581T>A	ENSP00000384582.2:p.Ser3527=
ENST00000509621.1:c.3278T>A
NM_032119.3:c.10581T>A	NP_115495.3:p.Ser3527=
NR_003149.1:n.10594T>A
XM_011543675.1:c.10578T>A	XP_011541977.1:p.Ser3526=
XM_011543676.1:c.10500T>A	XP_011541978.1:p.Ser3500=
XM_011543677.1:c.7884T>A	XP_011541979.1:p.Ser2628=
XM_011543678.1:c.10581T>A	XP_011541980.1:p.Ser3527=
XM_011543679.1:c.10581T>A	XP_011541981.1:p.Ser3527=
NM_032119.4:c.10581T>A MANE Select	NP_115495.3:p.Ser3527=
XM_017009963.2:c.10602T>A	XP_016865452.1:p.Ser3534=
XM_017009964.2:c.10599T>A	XP_016865453.1:p.Ser3533=
XM_017009965.1:c.10599T>A	XP_016865454.1:p.Ser3533=
XM_017009966.2:c.10521T>A	XP_016865455.1:p.Ser3507=
XM_017009967.1:c.10506T>A	XP_016865456.1:p.Ser3502=
XM_017009968.2:c.10602T>A	XP_016865457.1:p.Ser3534=
XM_017009969.2:c.10602T>A	XP_016865458.1:p.Ser3534=
XM_017009970.2:c.10602T>A	XP_016865459.1:p.Ser3534=
XM_017009971.2:c.10602T>A	XP_016865460.1:p.Ser3534=
XM_017009972.1:c.3720T>A	XP_016865461.1:p.Ser1240=
XM_017009973.1:c.3699T>A	XP_016865462.1:p.Ser1233=
XM_017009974.2:c.10602T>A	XP_016865463.1:p.Ser3534=
NR_003149.2:n.10597T>A