Canonical Allele Identifier: CA445406425

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90763346-A-C
• MyVariant Identifiers: chr5:g.90059163A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90763346A>C , CM000667.2:g.90763346A>C	GRCh38
NC_000005.9:g.90059163A>C , CM000667.1:g.90059163A>C	GRCh37
NC_000005.8:g.90094919A>C	NCBI36
NG_007083.1:g.209547A>C
NG_007083.2:g.239003A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.12162A>C MANE Select	ENSP00000384582.2:p.Ser4054=
ENST00000425867.3:c.1116A>C	ENSP00000392618.3:p.Ser372=
ENST00000639431.1:c.265+87137A>C	ENSP00000491057.1:n.265+87137A>C
ENST00000640464.1:n.2581A>C
ENST00000640729.1:n.739A>C
ENST00000405460.6:c.12162A>C	ENSP00000384582.2:p.Ser4054=
NM_032119.3:c.12162A>C	NP_115495.3:p.Ser4054=
NR_003149.1:n.12175A>C
XM_011543675.1:c.12159A>C	XP_011541977.1:p.Ser4053=
XM_011543676.1:c.12081A>C	XP_011541978.1:p.Ser4027=
XM_011543677.1:c.9465A>C	XP_011541979.1:p.Ser3155=
XM_011543678.1:c.12162A>C	XP_011541980.1:p.Ser4054=
NM_032119.4:c.12162A>C MANE Select	NP_115495.3:p.Ser4054=
XM_017009963.2:c.12183A>C	XP_016865452.1:p.Ser4061=
XM_017009964.2:c.12180A>C	XP_016865453.1:p.Ser4060=
XM_017009965.1:c.12180A>C	XP_016865454.1:p.Ser4060=
XM_017009966.2:c.12102A>C	XP_016865455.1:p.Ser4034=
XM_017009967.1:c.12087A>C	XP_016865456.1:p.Ser4029=
XM_017009968.2:c.12183A>C	XP_016865457.1:p.Ser4061=
XM_017009969.2:c.12183A>C	XP_016865458.1:p.Ser4061=
XM_017009970.2:c.12183A>C	XP_016865459.1:p.Ser4061=
XM_017009971.2:c.12183A>C	XP_016865460.1:p.Ser4061=
XM_017009972.1:c.5301A>C	XP_016865461.1:p.Ser1767=
XM_017009973.1:c.5280A>C	XP_016865462.1:p.Ser1760=
NR_003149.2:n.12178A>C