Canonical Allele Identifier: CA445406330

Gene: ADGRV1

Linked Data

• dbSNP Id: rs1363156948
• MyVariant Identifiers: chr5:g.90059130T>C (hg19) ; chr5:g.90763313T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90763313T>C , CM000667.2:g.90763313T>C	GRCh38
NC_000005.9:g.90059130T>C , CM000667.1:g.90059130T>C	GRCh37
NC_000005.8:g.90094886T>C	NCBI36
NG_007083.1:g.209514T>C
NG_007083.2:g.238970T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.12129T>C MANE Select	ENSP00000384582.2:p.Ile4043=
ENST00000425867.3:c.1083T>C	ENSP00000392618.3:p.Ile361=
ENST00000639431.1:c.265+87104T>C	ENSP00000491057.1:n.265+87104T>C
ENST00000640464.1:n.2548T>C
ENST00000640729.1:n.706T>C
ENST00000405460.6:c.12129T>C	ENSP00000384582.2:p.Ile4043=
NM_032119.3:c.12129T>C	NP_115495.3:p.Ile4043=
NR_003149.1:n.12142T>C
XM_011543675.1:c.12126T>C	XP_011541977.1:p.Ile4042=
XM_011543676.1:c.12048T>C	XP_011541978.1:p.Ile4016=
XM_011543677.1:c.9432T>C	XP_011541979.1:p.Ile3144=
XM_011543678.1:c.12129T>C	XP_011541980.1:p.Ile4043=
NM_032119.4:c.12129T>C MANE Select	NP_115495.3:p.Ile4043=
XM_017009963.2:c.12150T>C	XP_016865452.1:p.Ile4050=
XM_017009964.2:c.12147T>C	XP_016865453.1:p.Ile4049=
XM_017009965.1:c.12147T>C	XP_016865454.1:p.Ile4049=
XM_017009966.2:c.12069T>C	XP_016865455.1:p.Ile4023=
XM_017009967.1:c.12054T>C	XP_016865456.1:p.Ile4018=
XM_017009968.2:c.12150T>C	XP_016865457.1:p.Ile4050=
XM_017009969.2:c.12150T>C	XP_016865458.1:p.Ile4050=
XM_017009970.2:c.12150T>C	XP_016865459.1:p.Ile4050=
XM_017009971.2:c.12150T>C	XP_016865460.1:p.Ile4050=
XM_017009972.1:c.5268T>C	XP_016865461.1:p.Ile1756=
XM_017009973.1:c.5247T>C	XP_016865462.1:p.Ile1749=
NR_003149.2:n.12145T>C