Canonical Allele Identifier: CA445413918

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90012498G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716681G>A , CM000667.2:g.90716681G>A	GRCh38
NC_000005.9:g.90012498G>A , CM000667.1:g.90012498G>A	GRCh37
NC_000005.8:g.90048254G>A	NCBI36
NG_007083.1:g.162882G>A
NG_007083.2:g.192338G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9399G>A MANE Select	ENSP00000384582.2:p.Leu3133=
ENST00000639431.1:c.265+40472G>A	ENSP00000491057.1:n.265+40472G>A
ENST00000639473.1:n.4858G>A
ENST00000640012.1:c.3206G>A
ENST00000640374.1:n.2543G>A
ENST00000640779.1:c.4128G>A
ENST00000405460.6:c.9399G>A	ENSP00000384582.2:p.Leu3133=
ENST00000509621.1:c.2096G>A
NM_032119.3:c.9399G>A	NP_115495.3:p.Leu3133=
NR_003149.1:n.9412G>A
XM_011543675.1:c.9396G>A	XP_011541977.1:p.Leu3132=
XM_011543676.1:c.9318G>A	XP_011541978.1:p.Leu3106=
XM_011543677.1:c.6702G>A	XP_011541979.1:p.Leu2234=
XM_011543678.1:c.9399G>A	XP_011541980.1:p.Leu3133=
XM_011543679.1:c.9399G>A	XP_011541981.1:p.Leu3133=
XR_948560.1:n.272-872C>T
NM_032119.4:c.9399G>A MANE Select	NP_115495.3:p.Leu3133=
XM_017009963.2:c.9420G>A	XP_016865452.1:p.Leu3140=
XM_017009964.2:c.9417G>A	XP_016865453.1:p.Leu3139=
XM_017009965.1:c.9417G>A	XP_016865454.1:p.Leu3139=
XM_017009966.2:c.9339G>A	XP_016865455.1:p.Leu3113=
XM_017009967.1:c.9324G>A	XP_016865456.1:p.Leu3108=
XM_017009968.2:c.9420G>A	XP_016865457.1:p.Leu3140=
XM_017009969.2:c.9420G>A	XP_016865458.1:p.Leu3140=
XM_017009970.2:c.9420G>A	XP_016865459.1:p.Leu3140=
XM_017009971.2:c.9420G>A	XP_016865460.1:p.Leu3140=
XM_017009972.1:c.2538G>A	XP_016865461.1:p.Leu846=
XM_017009973.1:c.2517G>A	XP_016865462.1:p.Leu839=
XM_017009974.2:c.9420G>A	XP_016865463.1:p.Leu3140=
XR_001742802.1:n.2523-872C>T
NR_003149.2:n.9415G>A