Canonical Allele Identifier: CA360403783

Gene: ADGRV1

Linked Data

• dbSNP Id: rs1462565557
• gnomAD v2: 5-90024541-G-A
• gnomAD v3: 5-90728724-G-A
• gnomAD v4: 5-90728724-G-A
• MyVariant Identifiers: chr5:g.90024541G>A (hg19) ; chr5:g.90728724G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90728724G>A , CM000667.2:g.90728724G>A	GRCh38
NC_000005.9:g.90024541G>A , CM000667.1:g.90024541G>A	GRCh37
NC_000005.8:g.90060297G>A	NCBI36
NG_007083.1:g.174925G>A
NG_007083.2:g.204381G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10217G>A MANE Select	ENSP00000384582.2:p.Gly3406Asp
ENST00000639431.1:c.265+52515G>A	ENSP00000491057.1:n.265+52515G>A
ENST00000640374.1:n.3361G>A
ENST00000640464.1:n.636G>A
ENST00000405460.6:c.10217G>A	ENSP00000384582.2:p.Gly3406Asp
ENST00000509621.1:c.2914G>A
NM_032119.3:c.10217G>A	NP_115495.3:p.Gly3406Asp
NR_003149.1:n.10230G>A
XM_011543675.1:c.10214G>A	XP_011541977.1:p.Gly3405Asp
XM_011543676.1:c.10136G>A	XP_011541978.1:p.Gly3379Asp
XM_011543677.1:c.7520G>A	XP_011541979.1:p.Gly2507Asp
XM_011543678.1:c.10217G>A	XP_011541980.1:p.Gly3406Asp
XM_011543679.1:c.10217G>A	XP_011541981.1:p.Gly3406Asp
XR_948560.1:n.271+12183C>T
NM_032119.4:c.10217G>A MANE Select	NP_115495.3:p.Gly3406Asp
XM_017009963.2:c.10238G>A	XP_016865452.1:p.Gly3413Asp
XM_017009964.2:c.10235G>A	XP_016865453.1:p.Gly3412Asp
XM_017009965.1:c.10235G>A	XP_016865454.1:p.Gly3412Asp
XM_017009966.2:c.10157G>A	XP_016865455.1:p.Gly3386Asp
XM_017009967.1:c.10142G>A	XP_016865456.1:p.Gly3381Asp
XM_017009968.2:c.10238G>A	XP_016865457.1:p.Gly3413Asp
XM_017009969.2:c.10238G>A	XP_016865458.1:p.Gly3413Asp
XM_017009970.2:c.10238G>A	XP_016865459.1:p.Gly3413Asp
XM_017009971.2:c.10238G>A	XP_016865460.1:p.Gly3413Asp
XM_017009972.1:c.3356G>A	XP_016865461.1:p.Gly1119Asp
XM_017009973.1:c.3335G>A	XP_016865462.1:p.Gly1112Asp
XM_017009974.2:c.10238G>A	XP_016865463.1:p.Gly3413Asp
XR_001742802.1:n.2522+12183C>T
NR_003149.2:n.10233G>A