Canonical Allele Identifier: CA360414047

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89979800T>G (hg19) ; chr5:g.90683983T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90683983T>G , CM000667.2:g.90683983T>G	GRCh38
NC_000005.9:g.89979800T>G , CM000667.1:g.89979800T>G	GRCh37
NC_000005.8:g.90015556T>G	NCBI36
NG_007083.1:g.130184T>G
NG_007083.2:g.159640T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.6062T>G MANE Select	ENSP00000384582.2:p.Met2021Arg
ENST00000639431.1:c.265+7774T>G	ENSP00000491057.1:n.265+7774T>G
ENST00000639473.1:n.1521T>G
ENST00000640012.1:c.165-1797T>G
ENST00000640403.1:c.3353T>G	ENSP00000492531.1:p.Met1118Arg
ENST00000640779.1:c.874T>G
ENST00000405460.6:c.6062T>G	ENSP00000384582.2:p.Met2021Arg
NM_032119.3:c.6062T>G	NP_115495.3:p.Met2021Arg
NR_003149.1:n.6158T>G
XM_011543675.1:c.6059T>G	XP_011541977.1:p.Met2020Arg
XM_011543676.1:c.5981T>G	XP_011541978.1:p.Met1994Arg
XM_011543677.1:c.3365T>G	XP_011541979.1:p.Met1122Arg
XM_011543678.1:c.6062T>G	XP_011541980.1:p.Met2021Arg
XM_011543679.1:c.6062T>G	XP_011541981.1:p.Met2021Arg
NM_032119.4:c.6062T>G MANE Select	NP_115495.3:p.Met2021Arg
XM_017009963.2:c.6062T>G	XP_016865452.1:p.Met2021Arg
XM_017009964.2:c.6059T>G	XP_016865453.1:p.Met2020Arg
XM_017009965.1:c.6059T>G	XP_016865454.1:p.Met2020Arg
XM_017009966.2:c.5981T>G	XP_016865455.1:p.Met1994Arg
XM_017009967.1:c.5966T>G	XP_016865456.1:p.Met1989Arg
XM_017009968.2:c.6062T>G	XP_016865457.1:p.Met2021Arg
XM_017009969.2:c.6062T>G	XP_016865458.1:p.Met2021Arg
XM_017009970.2:c.6062T>G	XP_016865459.1:p.Met2021Arg
XM_017009971.2:c.6062T>G	XP_016865460.1:p.Met2021Arg
XM_017009973.1:c.-738T>G	XP_016865462.1:n.-738T>G
XM_017009974.2:c.6062T>G	XP_016865463.1:p.Met2021Arg
NR_003149.2:n.6161T>G