Canonical Allele Identifier: CA445416116

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90041498C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745681C>A , CM000667.2:g.90745681C>A	GRCh38
NC_000005.9:g.90041498C>A , CM000667.1:g.90041498C>A	GRCh37
NC_000005.8:g.90077254C>A	NCBI36
NG_007083.1:g.191882C>A
NG_007083.2:g.221338C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10860C>A MANE Select	ENSP00000384582.2:p.Ser3620=
ENST00000639431.1:c.265+69472C>A	ENSP00000491057.1:n.265+69472C>A
ENST00000640374.1:n.4004C>A
ENST00000640464.1:n.1279C>A
ENST00000405460.6:c.10860C>A	ENSP00000384582.2:p.Ser3620=
ENST00000509621.1:c.3557C>A
NM_032119.3:c.10860C>A	NP_115495.3:p.Ser3620=
NR_003149.1:n.10873C>A
XM_011543675.1:c.10857C>A	XP_011541977.1:p.Ser3619=
XM_011543676.1:c.10779C>A	XP_011541978.1:p.Ser3593=
XM_011543677.1:c.8163C>A	XP_011541979.1:p.Ser2721=
XM_011543678.1:c.10860C>A	XP_011541980.1:p.Ser3620=
XM_011543679.1:c.*82C>A	XP_011541981.1:n.*82C>A
NM_032119.4:c.10860C>A MANE Select	NP_115495.3:p.Ser3620=
XM_017009963.2:c.10881C>A	XP_016865452.1:p.Ser3627=
XM_017009964.2:c.10878C>A	XP_016865453.1:p.Ser3626=
XM_017009965.1:c.10878C>A	XP_016865454.1:p.Ser3626=
XM_017009966.2:c.10800C>A	XP_016865455.1:p.Ser3600=
XM_017009967.1:c.10785C>A	XP_016865456.1:p.Ser3595=
XM_017009968.2:c.10881C>A	XP_016865457.1:p.Ser3627=
XM_017009969.2:c.10881C>A	XP_016865458.1:p.Ser3627=
XM_017009970.2:c.10881C>A	XP_016865459.1:p.Ser3627=
XM_017009971.2:c.10881C>A	XP_016865460.1:p.Ser3627=
XM_017009972.1:c.3999C>A	XP_016865461.1:p.Ser1333=
XM_017009973.1:c.3978C>A	XP_016865462.1:p.Ser1326=
XM_017009974.2:c.*82C>A	XP_016865463.1:n.*82C>A
NR_003149.2:n.10876C>A