Canonical Allele Identifier: CA445467973

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90106719T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90810902T>G , CM000667.2:g.90810902T>G	GRCh38
NC_000005.9:g.90106719T>G , CM000667.1:g.90106719T>G	GRCh37
NC_000005.8:g.90142475T>G	NCBI36
NG_007083.1:g.257103T>G
NG_007083.2:g.286559T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.15642T>G MANE Select	ENSP00000384582.2:p.Val5214=
ENST00000425867.3:c.4596T>G	ENSP00000392618.3:p.Val1532=
ENST00000638510.1:n.2909T>G
ENST00000639431.1:c.265+134693T>G	ENSP00000491057.1:n.265+134693T>G
ENST00000640407.1:c.2052T>G	ENSP00000491425.1:p.Val684=
ENST00000405460.6:c.15642T>G	ENSP00000384582.2:p.Val5214=
ENST00000425867.2:c.2625T>G	ENSP00000392618.2:p.Val875=
NM_032119.3:c.15642T>G	NP_115495.3:p.Val5214=
NR_003149.1:n.15655T>G
XM_011543675.1:c.15639T>G	XP_011541977.1:p.Val5213=
XM_011543676.1:c.15561T>G	XP_011541978.1:p.Val5187=
XM_011543677.1:c.12945T>G	XP_011541979.1:p.Val4315=
NM_032119.4:c.15642T>G MANE Select	NP_115495.3:p.Val5214=
XM_017009963.2:c.15663T>G	XP_016865452.1:p.Val5221=
XM_017009964.2:c.15660T>G	XP_016865453.1:p.Val5220=
XM_017009965.1:c.15660T>G	XP_016865454.1:p.Val5220=
XM_017009966.2:c.15582T>G	XP_016865455.1:p.Val5194=
XM_017009967.1:c.15567T>G	XP_016865456.1:p.Val5189=
XM_017009968.2:c.15483T>G	XP_016865457.1:p.Val5161=
XM_017009969.2:c.15663T>G	XP_016865458.1:p.Val5221=
XM_017009972.1:c.8781T>G	XP_016865461.1:p.Val2927=
XM_017009973.1:c.8760T>G	XP_016865462.1:p.Val2920=
NR_003149.2:n.15658T>G