Canonical Allele Identifier: CA360396391

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90712414-G-A
• MyVariant Identifiers: chr5:g.90008231G>A (hg19) ; chr5:g.90712414G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712414G>A , CM000667.2:g.90712414G>A	GRCh38
NC_000005.9:g.90008231G>A , CM000667.1:g.90008231G>A	GRCh37
NC_000005.8:g.90043987G>A	NCBI36
NG_007083.1:g.158615G>A
NG_007083.2:g.188071G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9170G>A MANE Select	ENSP00000384582.2:p.Gly3057Glu
ENST00000639431.1:c.265+36205G>A	ENSP00000491057.1:n.265+36205G>A
ENST00000639473.1:n.4629G>A
ENST00000640012.1:c.2977G>A
ENST00000640374.1:n.2314G>A
ENST00000640779.1:c.3899G>A
ENST00000405460.6:c.9170G>A	ENSP00000384582.2:p.Gly3057Glu
ENST00000509621.1:c.1867G>A
NM_032119.3:c.9170G>A	NP_115495.3:p.Gly3057Glu
NR_003149.1:n.9183G>A
XM_011543675.1:c.9167G>A	XP_011541977.1:p.Gly3056Glu
XM_011543676.1:c.9089G>A	XP_011541978.1:p.Gly3030Glu
XM_011543677.1:c.6473G>A	XP_011541979.1:p.Gly2158Glu
XM_011543678.1:c.9170G>A	XP_011541980.1:p.Gly3057Glu
XM_011543679.1:c.9170G>A	XP_011541981.1:p.Gly3057Glu
XR_948560.1:n.437-5C>T
NM_032119.4:c.9170G>A MANE Select	NP_115495.3:p.Gly3057Glu
XM_017009963.2:c.9191G>A	XP_016865452.1:p.Gly3064Glu
XM_017009964.2:c.9188G>A	XP_016865453.1:p.Gly3063Glu
XM_017009965.1:c.9188G>A	XP_016865454.1:p.Gly3063Glu
XM_017009966.2:c.9110G>A	XP_016865455.1:p.Gly3037Glu
XM_017009967.1:c.9095G>A	XP_016865456.1:p.Gly3032Glu
XM_017009968.2:c.9191G>A	XP_016865457.1:p.Gly3064Glu
XM_017009969.2:c.9191G>A	XP_016865458.1:p.Gly3064Glu
XM_017009970.2:c.9191G>A	XP_016865459.1:p.Gly3064Glu
XM_017009971.2:c.9191G>A	XP_016865460.1:p.Gly3064Glu
XM_017009972.1:c.2309G>A	XP_016865461.1:p.Gly770Glu
XM_017009973.1:c.2288G>A	XP_016865462.1:p.Gly763Glu
XM_017009974.2:c.9191G>A	XP_016865463.1:p.Gly3064Glu
NR_003149.2:n.9186G>A