Canonical Allele Identifier: CA445468305

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90106827G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90811010G>C , CM000667.2:g.90811010G>C	GRCh38
NC_000005.9:g.90106827G>C , CM000667.1:g.90106827G>C	GRCh37
NC_000005.8:g.90142583G>C	NCBI36
NG_007083.1:g.257211G>C
NG_007083.2:g.286667G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.15750G>C MANE Select	ENSP00000384582.2:p.Gly5250=
ENST00000425867.3:c.4704G>C	ENSP00000392618.3:p.Gly1568=
ENST00000638510.1:n.3017G>C
ENST00000639431.1:c.265+134801G>C	ENSP00000491057.1:n.265+134801G>C
ENST00000640407.1:c.2160G>C	ENSP00000491425.1:p.Gly720=
ENST00000405460.6:c.15750G>C	ENSP00000384582.2:p.Gly5250=
ENST00000425867.2:c.2733G>C	ENSP00000392618.2:p.Gly911=
NM_032119.3:c.15750G>C	NP_115495.3:p.Gly5250=
NR_003149.1:n.15763G>C
XM_011543675.1:c.15747G>C	XP_011541977.1:p.Gly5249=
XM_011543676.1:c.15669G>C	XP_011541978.1:p.Gly5223=
XM_011543677.1:c.13053G>C	XP_011541979.1:p.Gly4351=
NM_032119.4:c.15750G>C MANE Select	NP_115495.3:p.Gly5250=
XM_017009963.2:c.15771G>C	XP_016865452.1:p.Gly5257=
XM_017009964.2:c.15768G>C	XP_016865453.1:p.Gly5256=
XM_017009965.1:c.15768G>C	XP_016865454.1:p.Gly5256=
XM_017009966.2:c.15690G>C	XP_016865455.1:p.Gly5230=
XM_017009967.1:c.15675G>C	XP_016865456.1:p.Gly5225=
XM_017009968.2:c.15591G>C	XP_016865457.1:p.Gly5197=
XM_017009969.2:c.15771G>C	XP_016865458.1:p.Gly5257=
XM_017009972.1:c.8889G>C	XP_016865461.1:p.Gly2963=
XM_017009973.1:c.8868G>C	XP_016865462.1:p.Gly2956=
NR_003149.2:n.15766G>C