Canonical Allele Identifier: CA360378190

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90763406G>A , CM000667.2:g.90763406G>A	GRCh38
NC_000005.9:g.90059223G>A , CM000667.1:g.90059223G>A	GRCh37
NC_000005.8:g.90094979G>A	NCBI36
NG_007083.1:g.209607G>A
NG_007083.2:g.239063G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.12222G>A MANE Select	NP_115495.3:p.Trp4074Ter
ENST00000405460.9:c.12222G>A MANE Select	ENSP00000384582.2:p.Trp4074Ter
NM_032119.3:c.12222G>A	NP_115495.3:p.Trp4074Ter
NR_003149.1:n.12235G>A
NR_003149.2:n.12238G>A
ENST00000405460.6:c.12222G>A	ENSP00000384582.2:p.Trp4074Ter
ENST00000425867.3:c.1176G>A	ENSP00000392618.3:p.Trp392Ter
ENST00000639431.1:c.265+87197G>A	ENSP00000491057.1:n.265+87197G>A
ENST00000640464.1:n.2641G>A
ENST00000640729.1:n.799G>A
XM_011543675.1:c.12219G>A	XP_011541977.1:p.Trp4073Ter
XM_011543676.1:c.12141G>A	XP_011541978.1:p.Trp4047Ter
XM_011543677.1:c.9525G>A	XP_011541979.1:p.Trp3175Ter
XM_011543678.1:c.12222G>A	XP_011541980.1:p.Trp4074Ter
XM_017009963.2:c.12243G>A	XP_016865452.1:p.Trp4081Ter
XM_017009964.2:c.12240G>A	XP_016865453.1:p.Trp4080Ter
XM_017009965.1:c.12240G>A	XP_016865454.1:p.Trp4080Ter
XM_017009966.2:c.12162G>A	XP_016865455.1:p.Trp4054Ter
XM_017009967.1:c.12147G>A	XP_016865456.1:p.Trp4049Ter
XM_017009968.2:c.12243G>A	XP_016865457.1:p.Trp4081Ter
XM_017009969.2:c.12243G>A	XP_016865458.1:p.Trp4081Ter
XM_017009970.2:c.12243G>A	XP_016865459.1:p.Trp4081Ter
XM_017009971.2:c.12243G>A	XP_016865460.1:p.Trp4081Ter
XM_017009972.1:c.5361G>A	XP_016865461.1:p.Trp1787Ter
XM_017009973.1:c.5340G>A	XP_016865462.1:p.Trp1780Ter