Canonical Allele Identifier: CA360425562

Gene: ADGRV1

Linked Data

• dbSNP Id: rs1455751241
• gnomAD v2: 5-90119304-A-G
• gnomAD v4: 5-90823487-A-G
• MyVariant Identifiers: chr5:g.90119304A>G (hg19) ; chr5:g.90823487A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823487A>G , CM000667.2:g.90823487A>G	GRCh38
NC_000005.9:g.90119304A>G , CM000667.1:g.90119304A>G	GRCh37
NC_000005.8:g.90155060A>G	NCBI36
NG_007083.1:g.269688A>G
NG_007083.2:g.299144A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.16259A>G MANE Select	ENSP00000384582.2:p.Gln5420Arg
ENST00000425867.3:c.5213A>G	ENSP00000392618.3:p.Gln1738Arg
ENST00000638510.1:n.3526A>G
ENST00000639431.1:c.265+147278A>G	ENSP00000491057.1:n.265+147278A>G
ENST00000640061.1:n.128+1305A>G
ENST00000640407.1:c.2669A>G	ENSP00000491425.1:p.Gln890Arg
ENST00000405460.6:c.16259A>G	ENSP00000384582.2:p.Gln5420Arg
ENST00000425867.2:c.3242A>G	ENSP00000392618.2:p.Gln1081Arg
NM_032119.3:c.16259A>G	NP_115495.3:p.Gln5420Arg
NR_003149.1:n.16272A>G
XM_011543675.1:c.16256A>G	XP_011541977.1:p.Gln5419Arg
XM_011543676.1:c.16178A>G	XP_011541978.1:p.Gln5393Arg
XM_011543677.1:c.13562A>G	XP_011541979.1:p.Gln4521Arg
NM_032119.4:c.16259A>G MANE Select	NP_115495.3:p.Gln5420Arg
XM_017009963.2:c.16280A>G	XP_016865452.1:p.Gln5427Arg
XM_017009964.2:c.16277A>G	XP_016865453.1:p.Gln5426Arg
XM_017009965.1:c.16277A>G	XP_016865454.1:p.Gln5426Arg
XM_017009966.2:c.16199A>G	XP_016865455.1:p.Gln5400Arg
XM_017009967.1:c.16184A>G	XP_016865456.1:p.Gln5395Arg
XM_017009968.2:c.16100A>G	XP_016865457.1:p.Gln5367Arg
XM_017009969.2:c.16280A>G	XP_016865458.1:p.Gln5427Arg
XM_017009972.1:c.9398A>G	XP_016865461.1:p.Gln3133Arg
XM_017009973.1:c.9377A>G	XP_016865462.1:p.Gln3126Arg
NR_003149.2:n.16275A>G