Canonical Allele Identifier: CA360397032

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716496G>A , CM000667.2:g.90716496G>A	GRCh38
NC_000005.9:g.90012313G>A , CM000667.1:g.90012313G>A	GRCh37
NC_000005.8:g.90048069G>A	NCBI36
NG_007083.1:g.162697G>A
NG_007083.2:g.192153G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.9214G>A MANE Select	NP_115495.3:p.Gly3072Ser
ENST00000405460.9:c.9214G>A MANE Select	ENSP00000384582.2:p.Gly3072Ser
NM_032119.3:c.9214G>A	NP_115495.3:p.Gly3072Ser
NR_003149.1:n.9227G>A
NR_003149.2:n.9230G>A
ENST00000405460.6:c.9214G>A	ENSP00000384582.2:p.Gly3072Ser
ENST00000509621.1:c.1911G>A
ENST00000639431.1:c.265+40287G>A	ENSP00000491057.1:n.265+40287G>A
ENST00000639473.1:n.4673G>A
ENST00000640012.1:c.3021G>A
ENST00000640374.1:n.2358G>A
ENST00000640779.1:c.3943G>A
XM_011543675.1:c.9211G>A	XP_011541977.1:p.Gly3071Ser
XM_011543676.1:c.9133G>A	XP_011541978.1:p.Gly3045Ser
XM_011543677.1:c.6517G>A	XP_011541979.1:p.Gly2173Ser
XM_011543678.1:c.9214G>A	XP_011541980.1:p.Gly3072Ser
XM_011543679.1:c.9214G>A	XP_011541981.1:p.Gly3072Ser
XM_017009963.2:c.9235G>A	XP_016865452.1:p.Gly3079Ser
XM_017009964.2:c.9232G>A	XP_016865453.1:p.Gly3078Ser
XM_017009965.1:c.9232G>A	XP_016865454.1:p.Gly3078Ser
XM_017009966.2:c.9154G>A	XP_016865455.1:p.Gly3052Ser
XM_017009967.1:c.9139G>A	XP_016865456.1:p.Gly3047Ser
XM_017009968.2:c.9235G>A	XP_016865457.1:p.Gly3079Ser
XM_017009969.2:c.9235G>A	XP_016865458.1:p.Gly3079Ser
XM_017009970.2:c.9235G>A	XP_016865459.1:p.Gly3079Ser
XM_017009971.2:c.9235G>A	XP_016865460.1:p.Gly3079Ser
XM_017009972.1:c.2353G>A	XP_016865461.1:p.Gly785Ser
XM_017009973.1:c.2332G>A	XP_016865462.1:p.Gly778Ser
XM_017009974.2:c.9235G>A	XP_016865463.1:p.Gly3079Ser
XR_001742802.1:n.2523-687C>T
XR_948560.1:n.272-687C>T