Canonical Allele Identifier: CA360366877

Gene: ADGRV1

Linked Data

• dbSNP Id: rs1755688624
• gnomAD v3: 5-90755094-C-T
• gnomAD v4: 5-90755094-C-T
• MyVariant Identifiers: chr5:g.90050911C>T (hg19) ; chr5:g.90755094C>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11489C>T MANE Select	ENSP00000384582.2:p.Ala3830Val
ENST00000425867.3:c.620C>T	ENSP00000392618.3:p.Ala207Val
ENST00000639431.1:c.265+78885C>T	ENSP00000491057.1:n.265+78885C>T
ENST00000640374.1:n.4633C>T
ENST00000640464.1:n.1908C>T
ENST00000405460.6:c.11489C>T	ENSP00000384582.2:p.Ala3830Val
ENST00000509621.1:c.4186C>T
NM_032119.3:c.11489C>T	NP_115495.3:p.Ala3830Val
NR_003149.1:n.11502C>T
XM_011543675.1:c.11486C>T	XP_011541977.1:p.Ala3829Val
XM_011543676.1:c.11408C>T	XP_011541978.1:p.Ala3803Val
XM_011543677.1:c.8792C>T	XP_011541979.1:p.Ala2931Val
XM_011543678.1:c.11489C>T	XP_011541980.1:p.Ala3830Val
NM_032119.4:c.11489C>T MANE Select	NP_115495.3:p.Ala3830Val
XM_017009963.2:c.11510C>T	XP_016865452.1:p.Ala3837Val
XM_017009964.2:c.11507C>T	XP_016865453.1:p.Ala3836Val
XM_017009965.1:c.11507C>T	XP_016865454.1:p.Ala3836Val
XM_017009966.2:c.11429C>T	XP_016865455.1:p.Ala3810Val
XM_017009967.1:c.11414C>T	XP_016865456.1:p.Ala3805Val
XM_017009968.2:c.11510C>T	XP_016865457.1:p.Ala3837Val
XM_017009969.2:c.11510C>T	XP_016865458.1:p.Ala3837Val
XM_017009970.2:c.11510C>T	XP_016865459.1:p.Ala3837Val
XM_017009971.2:c.11510C>T	XP_016865460.1:p.Ala3837Val
XM_017009972.1:c.4628C>T	XP_016865461.1:p.Ala1543Val
XM_017009973.1:c.4607C>T	XP_016865462.1:p.Ala1536Val
NR_003149.2:n.11505C>T