Canonical Allele Identifier: CA445436601

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119371T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823554T>G , CM000667.2:g.90823554T>G	GRCh38
NC_000005.9:g.90119371T>G , CM000667.1:g.90119371T>G	GRCh37
NC_000005.8:g.90155127T>G	NCBI36
NG_007083.1:g.269755T>G
NG_007083.2:g.299211T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16326T>G MANE Select	ENSP00000384582.2:p.Gly5442=
ENST00000425867.3:c.5280T>G	ENSP00000392618.3:p.Gly1760=
ENST00000638510.1:n.3593T>G
ENST00000639431.1:c.265+147345T>G	ENSP00000491057.1:n.265+147345T>G
ENST00000640061.1:n.128+1372T>G
ENST00000640407.1:c.2736T>G	ENSP00000491425.1:p.Gly912=
ENST00000405460.6:c.16326T>G	ENSP00000384582.2:p.Gly5442=
ENST00000425867.2:c.3309T>G	ENSP00000392618.2:p.Gly1103=
NM_032119.3:c.16326T>G	NP_115495.3:p.Gly5442=
NR_003149.1:n.16339T>G
XM_011543675.1:c.16323T>G	XP_011541977.1:p.Gly5441=
XM_011543676.1:c.16245T>G	XP_011541978.1:p.Gly5415=
XM_011543677.1:c.13629T>G	XP_011541979.1:p.Gly4543=
NM_032119.4:c.16326T>G MANE Select	NP_115495.3:p.Gly5442=
XM_017009963.2:c.16347T>G	XP_016865452.1:p.Gly5449=
XM_017009964.2:c.16344T>G	XP_016865453.1:p.Gly5448=
XM_017009965.1:c.16344T>G	XP_016865454.1:p.Gly5448=
XM_017009966.2:c.16266T>G	XP_016865455.1:p.Gly5422=
XM_017009967.1:c.16251T>G	XP_016865456.1:p.Gly5417=
XM_017009968.2:c.16167T>G	XP_016865457.1:p.Gly5389=
XM_017009969.2:c.16347T>G	XP_016865458.1:p.Gly5449=
XM_017009972.1:c.9465T>G	XP_016865461.1:p.Gly3155=
XM_017009973.1:c.9444T>G	XP_016865462.1:p.Gly3148=
NR_003149.2:n.16342T>G