Canonical Allele Identifier: CA360366263

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050819G>C (hg19) ; chr5:g.90755002G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755002G>C , CM000667.2:g.90755002G>C	GRCh38
NC_000005.9:g.90050819G>C , CM000667.1:g.90050819G>C	GRCh37
NC_000005.8:g.90086575G>C	NCBI36
NG_007083.1:g.201203G>C
NG_007083.2:g.230659G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11397G>C MANE Select	ENSP00000384582.2:p.Gln3799His
ENST00000425867.3:c.528G>C	ENSP00000392618.3:p.Gln176His
ENST00000639431.1:c.265+78793G>C	ENSP00000491057.1:n.265+78793G>C
ENST00000640374.1:n.4541G>C
ENST00000640464.1:n.1816G>C
ENST00000405460.6:c.11397G>C	ENSP00000384582.2:p.Gln3799His
ENST00000509621.1:c.4094G>C
NM_032119.3:c.11397G>C	NP_115495.3:p.Gln3799His
NR_003149.1:n.11410G>C
XM_011543675.1:c.11394G>C	XP_011541977.1:p.Gln3798His
XM_011543676.1:c.11316G>C	XP_011541978.1:p.Gln3772His
XM_011543677.1:c.8700G>C	XP_011541979.1:p.Gln2900His
XM_011543678.1:c.11397G>C	XP_011541980.1:p.Gln3799His
NM_032119.4:c.11397G>C MANE Select	NP_115495.3:p.Gln3799His
XM_017009963.2:c.11418G>C	XP_016865452.1:p.Gln3806His
XM_017009964.2:c.11415G>C	XP_016865453.1:p.Gln3805His
XM_017009965.1:c.11415G>C	XP_016865454.1:p.Gln3805His
XM_017009966.2:c.11337G>C	XP_016865455.1:p.Gln3779His
XM_017009967.1:c.11322G>C	XP_016865456.1:p.Gln3774His
XM_017009968.2:c.11418G>C	XP_016865457.1:p.Gln3806His
XM_017009969.2:c.11418G>C	XP_016865458.1:p.Gln3806His
XM_017009970.2:c.11418G>C	XP_016865459.1:p.Gln3806His
XM_017009971.2:c.11418G>C	XP_016865460.1:p.Gln3806His
XM_017009972.1:c.4536G>C	XP_016865461.1:p.Gln1512His
XM_017009973.1:c.4515G>C	XP_016865462.1:p.Gln1505His
NR_003149.2:n.11413G>C