Canonical Allele Identifier: CA360366879

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90755094-C-A
• MyVariant Identifiers: chr5:g.90050911C>A (hg19) ; chr5:g.90755094C>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11489C>A MANE Select	ENSP00000384582.2:p.Ala3830Asp
ENST00000425867.3:c.620C>A	ENSP00000392618.3:p.Ala207Asp
ENST00000639431.1:c.265+78885C>A	ENSP00000491057.1:n.265+78885C>A
ENST00000640374.1:n.4633C>A
ENST00000640464.1:n.1908C>A
ENST00000405460.6:c.11489C>A	ENSP00000384582.2:p.Ala3830Asp
ENST00000509621.1:c.4186C>A
NM_032119.3:c.11489C>A	NP_115495.3:p.Ala3830Asp
NR_003149.1:n.11502C>A
XM_011543675.1:c.11486C>A	XP_011541977.1:p.Ala3829Asp
XM_011543676.1:c.11408C>A	XP_011541978.1:p.Ala3803Asp
XM_011543677.1:c.8792C>A	XP_011541979.1:p.Ala2931Asp
XM_011543678.1:c.11489C>A	XP_011541980.1:p.Ala3830Asp
NM_032119.4:c.11489C>A MANE Select	NP_115495.3:p.Ala3830Asp
XM_017009963.2:c.11510C>A	XP_016865452.1:p.Ala3837Asp
XM_017009964.2:c.11507C>A	XP_016865453.1:p.Ala3836Asp
XM_017009965.1:c.11507C>A	XP_016865454.1:p.Ala3836Asp
XM_017009966.2:c.11429C>A	XP_016865455.1:p.Ala3810Asp
XM_017009967.1:c.11414C>A	XP_016865456.1:p.Ala3805Asp
XM_017009968.2:c.11510C>A	XP_016865457.1:p.Ala3837Asp
XM_017009969.2:c.11510C>A	XP_016865458.1:p.Ala3837Asp
XM_017009970.2:c.11510C>A	XP_016865459.1:p.Ala3837Asp
XM_017009971.2:c.11510C>A	XP_016865460.1:p.Ala3837Asp
XM_017009972.1:c.4628C>A	XP_016865461.1:p.Ala1543Asp
XM_017009973.1:c.4607C>A	XP_016865462.1:p.Ala1536Asp
NR_003149.2:n.11505C>A