Canonical Allele Identifier: CA122804774

Gene: ADGRV1

Linked Data

• dbSNP Id: rs943597822
• MyVariant Identifiers: chr5:g.90008230G>C (hg19) ; chr5:g.90712413G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712413G>C , CM000667.2:g.90712413G>C	GRCh38
NC_000005.9:g.90008230G>C , CM000667.1:g.90008230G>C	GRCh37
NC_000005.8:g.90043986G>C	NCBI36
NG_007083.1:g.158614G>C
NG_007083.2:g.188070G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9169G>C MANE Select	ENSP00000384582.2:p.Gly3057Arg
ENST00000639431.1:c.265+36204G>C	ENSP00000491057.1:n.265+36204G>C
ENST00000639473.1:n.4628G>C
ENST00000640012.1:c.2976G>C
ENST00000640374.1:n.2313G>C
ENST00000640779.1:c.3898G>C
ENST00000405460.6:c.9169G>C	ENSP00000384582.2:p.Gly3057Arg
ENST00000509621.1:c.1866G>C
NM_032119.3:c.9169G>C	NP_115495.3:p.Gly3057Arg
NR_003149.1:n.9182G>C
XM_011543675.1:c.9166G>C	XP_011541977.1:p.Gly3056Arg
XM_011543676.1:c.9088G>C	XP_011541978.1:p.Gly3030Arg
XM_011543677.1:c.6472G>C	XP_011541979.1:p.Gly2158Arg
XM_011543678.1:c.9169G>C	XP_011541980.1:p.Gly3057Arg
XM_011543679.1:c.9169G>C	XP_011541981.1:p.Gly3057Arg
XR_948560.1:n.437-4C>G
NM_032119.4:c.9169G>C MANE Select	NP_115495.3:p.Gly3057Arg
XM_017009963.2:c.9190G>C	XP_016865452.1:p.Gly3064Arg
XM_017009964.2:c.9187G>C	XP_016865453.1:p.Gly3063Arg
XM_017009965.1:c.9187G>C	XP_016865454.1:p.Gly3063Arg
XM_017009966.2:c.9109G>C	XP_016865455.1:p.Gly3037Arg
XM_017009967.1:c.9094G>C	XP_016865456.1:p.Gly3032Arg
XM_017009968.2:c.9190G>C	XP_016865457.1:p.Gly3064Arg
XM_017009969.2:c.9190G>C	XP_016865458.1:p.Gly3064Arg
XM_017009970.2:c.9190G>C	XP_016865459.1:p.Gly3064Arg
XM_017009971.2:c.9190G>C	XP_016865460.1:p.Gly3064Arg
XM_017009972.1:c.2308G>C	XP_016865461.1:p.Gly770Arg
XM_017009973.1:c.2287G>C	XP_016865462.1:p.Gly763Arg
XM_017009974.2:c.9190G>C	XP_016865463.1:p.Gly3064Arg
NR_003149.2:n.9185G>C