Canonical Allele Identifier: CA3341153

Gene: ADGRV1

Linked Data

• dbSNP Id: rs767584003
• ExAC: 5:90059103 C / G
• gnomAD v2: 5-90059103-C-G
• gnomAD v4: 5-90763286-C-G
• MyVariant Identifiers: chr5:g.90059103C>G (hg19) ; chr5:g.90763286C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90763286C>G , CM000667.2:g.90763286C>G	GRCh38
NC_000005.9:g.90059103C>G , CM000667.1:g.90059103C>G	GRCh37
NC_000005.8:g.90094859C>G	NCBI36
NG_007083.1:g.209487C>G
NG_007083.2:g.238943C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.12121-19C>G MANE Select	ENSP00000384582.2:n.12121-19C>G
ENST00000425867.3:c.1075-19C>G	ENSP00000392618.3:n.1075-19C>G
ENST00000639431.1:c.265+87077C>G	ENSP00000491057.1:n.265+87077C>G
ENST00000640464.1:n.2540-19C>G
ENST00000640729.1:n.679C>G
ENST00000405460.6:c.12121-19C>G	ENSP00000384582.2:n.12121-19C>G
NM_032119.3:c.12121-19C>G	NP_115495.3:n.12121-19C>G
NR_003149.1:n.12134-19C>G
XM_011543675.1:c.12118-19C>G	XP_011541977.1:n.12118-19C>G
XM_011543676.1:c.12040-19C>G	XP_011541978.1:n.12040-19C>G
XM_011543677.1:c.9424-19C>G	XP_011541979.1:n.9424-19C>G
XM_011543678.1:c.12121-19C>G	XP_011541980.1:n.12121-19C>G
NM_032119.4:c.12121-19C>G MANE Select	NP_115495.3:n.12121-19C>G
XM_017009963.2:c.12142-19C>G	XP_016865452.1:n.12142-19C>G
XM_017009964.2:c.12139-19C>G	XP_016865453.1:n.12139-19C>G
XM_017009965.1:c.12139-19C>G	XP_016865454.1:n.12139-19C>G
XM_017009966.2:c.12061-19C>G	XP_016865455.1:n.12061-19C>G
XM_017009967.1:c.12046-19C>G	XP_016865456.1:n.12046-19C>G
XM_017009968.2:c.12142-19C>G	XP_016865457.1:n.12142-19C>G
XM_017009969.2:c.12142-19C>G	XP_016865458.1:n.12142-19C>G
XM_017009970.2:c.12142-19C>G	XP_016865459.1:n.12142-19C>G
XM_017009971.2:c.12142-19C>G	XP_016865460.1:n.12142-19C>G
XM_017009972.1:c.5260-19C>G	XP_016865461.1:n.5260-19C>G
XM_017009973.1:c.5239-19C>G	XP_016865462.1:n.5239-19C>G
NR_003149.2:n.12137-19C>G