Canonical Allele Identifier: CA3340570

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90720972G>A , CM000667.2:g.90720972G>A	GRCh38
NC_000005.9:g.90016789G>A , CM000667.1:g.90016789G>A	GRCh37
NC_000005.8:g.90052545G>A	NCBI36
NG_007083.1:g.167173G>A
NG_007083.2:g.196629G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.9661G>A MANE Select	NP_115495.3:p.Val3221Met
ENST00000405460.9:c.9661G>A MANE Select	ENSP00000384582.2:p.Val3221Met
NM_032119.3:c.9661G>A	NP_115495.3:p.Val3221Met
NR_003149.1:n.9674G>A
NR_003149.2:n.9677G>A
ENST00000405460.6:c.9661G>A	ENSP00000384582.2:p.Val3221Met
ENST00000509621.1:c.2358G>A
ENST00000639431.1:c.265+44763G>A	ENSP00000491057.1:n.265+44763G>A
ENST00000640374.1:n.2805G>A
ENST00000640464.1:n.80G>A
ENST00000640779.1:c.4390G>A
XM_011543675.1:c.9658G>A	XP_011541977.1:p.Val3220Met
XM_011543676.1:c.9580G>A	XP_011541978.1:p.Val3194Met
XM_011543677.1:c.6964G>A	XP_011541979.1:p.Val2322Met
XM_011543678.1:c.9661G>A	XP_011541980.1:p.Val3221Met
XM_011543679.1:c.9661G>A	XP_011541981.1:p.Val3221Met
XM_017009963.2:c.9682G>A	XP_016865452.1:p.Val3228Met
XM_017009964.2:c.9679G>A	XP_016865453.1:p.Val3227Met
XM_017009965.1:c.9679G>A	XP_016865454.1:p.Val3227Met
XM_017009966.2:c.9601G>A	XP_016865455.1:p.Val3201Met
XM_017009967.1:c.9586G>A	XP_016865456.1:p.Val3196Met
XM_017009968.2:c.9682G>A	XP_016865457.1:p.Val3228Met
XM_017009969.2:c.9682G>A	XP_016865458.1:p.Val3228Met
XM_017009970.2:c.9682G>A	XP_016865459.1:p.Val3228Met
XM_017009971.2:c.9682G>A	XP_016865460.1:p.Val3228Met
XM_017009972.1:c.2800G>A	XP_016865461.1:p.Val934Met
XM_017009973.1:c.2779G>A	XP_016865462.1:p.Val927Met
XM_017009974.2:c.9682G>A	XP_016865463.1:p.Val3228Met
XR_001742802.1:n.2523-5163C>T
XR_948560.1:n.272-5163C>T