Canonical Allele Identifier: CA445468291

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90106824T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90811007T>C , CM000667.2:g.90811007T>C	GRCh38
NC_000005.9:g.90106824T>C , CM000667.1:g.90106824T>C	GRCh37
NC_000005.8:g.90142580T>C	NCBI36
NG_007083.1:g.257208T>C
NG_007083.2:g.286664T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.15747T>C MANE Select	ENSP00000384582.2:p.Gly5249=
ENST00000425867.3:c.4701T>C	ENSP00000392618.3:p.Gly1567=
ENST00000638510.1:n.3014T>C
ENST00000639431.1:c.265+134798T>C	ENSP00000491057.1:n.265+134798T>C
ENST00000640407.1:c.2157T>C	ENSP00000491425.1:p.Gly719=
ENST00000405460.6:c.15747T>C	ENSP00000384582.2:p.Gly5249=
ENST00000425867.2:c.2730T>C	ENSP00000392618.2:p.Gly910=
NM_032119.3:c.15747T>C	NP_115495.3:p.Gly5249=
NR_003149.1:n.15760T>C
XM_011543675.1:c.15744T>C	XP_011541977.1:p.Gly5248=
XM_011543676.1:c.15666T>C	XP_011541978.1:p.Gly5222=
XM_011543677.1:c.13050T>C	XP_011541979.1:p.Gly4350=
NM_032119.4:c.15747T>C MANE Select	NP_115495.3:p.Gly5249=
XM_017009963.2:c.15768T>C	XP_016865452.1:p.Gly5256=
XM_017009964.2:c.15765T>C	XP_016865453.1:p.Gly5255=
XM_017009965.1:c.15765T>C	XP_016865454.1:p.Gly5255=
XM_017009966.2:c.15687T>C	XP_016865455.1:p.Gly5229=
XM_017009967.1:c.15672T>C	XP_016865456.1:p.Gly5224=
XM_017009968.2:c.15588T>C	XP_016865457.1:p.Gly5196=
XM_017009969.2:c.15768T>C	XP_016865458.1:p.Gly5256=
XM_017009972.1:c.8886T>C	XP_016865461.1:p.Gly2962=
XM_017009973.1:c.8865T>C	XP_016865462.1:p.Gly2955=
NR_003149.2:n.15763T>C