Canonical Allele Identifier: CA360414227

Gene: ADGRV1

Linked Data

• dbSNP Id: rs1164801118
• MyVariant Identifiers: chr5:g.89979886G>A (hg19) ; chr5:g.90684069G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90684069G>A , CM000667.2:g.90684069G>A	GRCh38
NC_000005.9:g.89979886G>A , CM000667.1:g.89979886G>A	GRCh37
NC_000005.8:g.90015642G>A	NCBI36
NG_007083.1:g.130270G>A
NG_007083.2:g.159726G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.6148G>A MANE Select	ENSP00000384582.2:p.Gly2050Arg
ENST00000639431.1:c.265+7860G>A	ENSP00000491057.1:n.265+7860G>A
ENST00000639473.1:n.1607G>A
ENST00000640012.1:c.165-1711G>A
ENST00000640403.1:c.3439G>A	ENSP00000492531.1:p.Gly1147Arg
ENST00000640779.1:c.960G>A
ENST00000405460.6:c.6148G>A	ENSP00000384582.2:p.Gly2050Arg
NM_032119.3:c.6148G>A	NP_115495.3:p.Gly2050Arg
NR_003149.1:n.6244G>A
XM_011543675.1:c.6145G>A	XP_011541977.1:p.Gly2049Arg
XM_011543676.1:c.6067G>A	XP_011541978.1:p.Gly2023Arg
XM_011543677.1:c.3451G>A	XP_011541979.1:p.Gly1151Arg
XM_011543678.1:c.6148G>A	XP_011541980.1:p.Gly2050Arg
XM_011543679.1:c.6148G>A	XP_011541981.1:p.Gly2050Arg
NM_032119.4:c.6148G>A MANE Select	NP_115495.3:p.Gly2050Arg
XM_017009963.2:c.6148G>A	XP_016865452.1:p.Gly2050Arg
XM_017009964.2:c.6145G>A	XP_016865453.1:p.Gly2049Arg
XM_017009965.1:c.6145G>A	XP_016865454.1:p.Gly2049Arg
XM_017009966.2:c.6067G>A	XP_016865455.1:p.Gly2023Arg
XM_017009967.1:c.6052G>A	XP_016865456.1:p.Gly2018Arg
XM_017009968.2:c.6148G>A	XP_016865457.1:p.Gly2050Arg
XM_017009969.2:c.6148G>A	XP_016865458.1:p.Gly2050Arg
XM_017009970.2:c.6148G>A	XP_016865459.1:p.Gly2050Arg
XM_017009971.2:c.6148G>A	XP_016865460.1:p.Gly2050Arg
XM_017009973.1:c.-652G>A	XP_016865462.1:n.-652G>A
XM_017009974.2:c.6148G>A	XP_016865463.1:p.Gly2050Arg
NR_003149.2:n.6247G>A