Canonical Allele Identifier: CA1562918272

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823495G= , CM000667.2:g.90823495G=	GRCh38
NC_000005.9:g.90119312G= , CM000667.1:g.90119312G=	GRCh37
NC_000005.8:g.90155068G=	NCBI36
NG_007083.1:g.269696G=
NG_007083.2:g.299152G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16267G= MANE Select	ENSP00000384582.2:p.Gly5423=
ENST00000425867.3:c.5221G=	ENSP00000392618.3:p.Gly1741=
ENST00000638510.1:n.3534G=
ENST00000639431.1:c.265+147286G=	ENSP00000491057.1:n.265+147286G=
ENST00000640061.1:n.128+1313G=
ENST00000640407.1:c.2677G=	ENSP00000491425.1:p.Gly893=
ENST00000405460.6:c.16267G=	ENSP00000384582.2:p.Gly5423=
ENST00000425867.2:c.3250G=	ENSP00000392618.2:p.Gly1084=
NM_032119.3:c.16267G=	NP_115495.3:p.Gly5423=
NR_003149.1:n.16280G=
XM_011543675.1:c.16264G=	XP_011541977.1:p.Gly5422=
XM_011543676.1:c.16186G=	XP_011541978.1:p.Gly5396=
XM_011543677.1:c.13570G=	XP_011541979.1:p.Gly4524=
NM_032119.4:c.16267G= MANE Select	NP_115495.3:p.Gly5423=
XM_017009963.2:c.16288G=	XP_016865452.1:p.Gly5430=
XM_017009964.2:c.16285G=	XP_016865453.1:p.Gly5429=
XM_017009965.1:c.16285G=	XP_016865454.1:p.Gly5429=
XM_017009966.2:c.16207G=	XP_016865455.1:p.Gly5403=
XM_017009967.1:c.16192G=	XP_016865456.1:p.Gly5398=
XM_017009968.2:c.16108G=	XP_016865457.1:p.Gly5370=
XM_017009969.2:c.16288G=	XP_016865458.1:p.Gly5430=
XM_017009972.1:c.9406G=	XP_016865461.1:p.Gly3136=
XM_017009973.1:c.9385G=	XP_016865462.1:p.Gly3129=
NR_003149.2:n.16283G=