Canonical Allele Identifier: CA360410723

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90811008-G-A
• MyVariant Identifiers: chr5:g.90106825G>A (hg19) ; chr5:g.90811008G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90811008G>A , CM000667.2:g.90811008G>A	GRCh38
NC_000005.9:g.90106825G>A , CM000667.1:g.90106825G>A	GRCh37
NC_000005.8:g.90142581G>A	NCBI36
NG_007083.1:g.257209G>A
NG_007083.2:g.286665G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.15748G>A MANE Select	ENSP00000384582.2:p.Gly5250Arg
ENST00000425867.3:c.4702G>A	ENSP00000392618.3:p.Gly1568Arg
ENST00000638510.1:n.3015G>A
ENST00000639431.1:c.265+134799G>A	ENSP00000491057.1:n.265+134799G>A
ENST00000640407.1:c.2158G>A	ENSP00000491425.1:p.Gly720Arg
ENST00000405460.6:c.15748G>A	ENSP00000384582.2:p.Gly5250Arg
ENST00000425867.2:c.2731G>A	ENSP00000392618.2:p.Gly911Arg
NM_032119.3:c.15748G>A	NP_115495.3:p.Gly5250Arg
NR_003149.1:n.15761G>A
XM_011543675.1:c.15745G>A	XP_011541977.1:p.Gly5249Arg
XM_011543676.1:c.15667G>A	XP_011541978.1:p.Gly5223Arg
XM_011543677.1:c.13051G>A	XP_011541979.1:p.Gly4351Arg
NM_032119.4:c.15748G>A MANE Select	NP_115495.3:p.Gly5250Arg
XM_017009963.2:c.15769G>A	XP_016865452.1:p.Gly5257Arg
XM_017009964.2:c.15766G>A	XP_016865453.1:p.Gly5256Arg
XM_017009965.1:c.15766G>A	XP_016865454.1:p.Gly5256Arg
XM_017009966.2:c.15688G>A	XP_016865455.1:p.Gly5230Arg
XM_017009967.1:c.15673G>A	XP_016865456.1:p.Gly5225Arg
XM_017009968.2:c.15589G>A	XP_016865457.1:p.Gly5197Arg
XM_017009969.2:c.15769G>A	XP_016865458.1:p.Gly5257Arg
XM_017009972.1:c.8887G>A	XP_016865461.1:p.Gly2963Arg
XM_017009973.1:c.8866G>A	XP_016865462.1:p.Gly2956Arg
NR_003149.2:n.15764G>A