Canonical Allele Identifier: CA445436569

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119326G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823509G>C , CM000667.2:g.90823509G>C	GRCh38
NC_000005.9:g.90119326G>C , CM000667.1:g.90119326G>C	GRCh37
NC_000005.8:g.90155082G>C	NCBI36
NG_007083.1:g.269710G>C
NG_007083.2:g.299166G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16281G>C MANE Select	ENSP00000384582.2:p.Val5427=
ENST00000425867.3:c.5235G>C	ENSP00000392618.3:p.Val1745=
ENST00000638510.1:n.3548G>C
ENST00000639431.1:c.265+147300G>C	ENSP00000491057.1:n.265+147300G>C
ENST00000640061.1:n.128+1327G>C
ENST00000640407.1:c.2691G>C	ENSP00000491425.1:p.Val897=
ENST00000405460.6:c.16281G>C	ENSP00000384582.2:p.Val5427=
ENST00000425867.2:c.3264G>C	ENSP00000392618.2:p.Val1088=
NM_032119.3:c.16281G>C	NP_115495.3:p.Val5427=
NR_003149.1:n.16294G>C
XM_011543675.1:c.16278G>C	XP_011541977.1:p.Val5426=
XM_011543676.1:c.16200G>C	XP_011541978.1:p.Val5400=
XM_011543677.1:c.13584G>C	XP_011541979.1:p.Val4528=
NM_032119.4:c.16281G>C MANE Select	NP_115495.3:p.Val5427=
XM_017009963.2:c.16302G>C	XP_016865452.1:p.Val5434=
XM_017009964.2:c.16299G>C	XP_016865453.1:p.Val5433=
XM_017009965.1:c.16299G>C	XP_016865454.1:p.Val5433=
XM_017009966.2:c.16221G>C	XP_016865455.1:p.Val5407=
XM_017009967.1:c.16206G>C	XP_016865456.1:p.Val5402=
XM_017009968.2:c.16122G>C	XP_016865457.1:p.Val5374=
XM_017009969.2:c.16302G>C	XP_016865458.1:p.Val5434=
XM_017009972.1:c.9420G>C	XP_016865461.1:p.Val3140=
XM_017009973.1:c.9399G>C	XP_016865462.1:p.Val3133=
NR_003149.2:n.16297G>C