Canonical Allele Identifier: CA1562918267

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823488G= , CM000667.2:g.90823488G=	GRCh38
NC_000005.9:g.90119305G= , CM000667.1:g.90119305G=	GRCh37
NC_000005.8:g.90155061G=	NCBI36
NG_007083.1:g.269689G=
NG_007083.2:g.299145G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16260G= MANE Select	ENSP00000384582.2:p.Gln5420=
ENST00000425867.3:c.5214G=	ENSP00000392618.3:p.Gln1738=
ENST00000638510.1:n.3527G=
ENST00000639431.1:c.265+147279G=	ENSP00000491057.1:n.265+147279G=
ENST00000640061.1:n.128+1306G=
ENST00000640407.1:c.2670G=	ENSP00000491425.1:p.Gln890=
ENST00000405460.6:c.16260G=	ENSP00000384582.2:p.Gln5420=
ENST00000425867.2:c.3243G=	ENSP00000392618.2:p.Gln1081=
NM_032119.3:c.16260G=	NP_115495.3:p.Gln5420=
NR_003149.1:n.16273G=
XM_011543675.1:c.16257G=	XP_011541977.1:p.Gln5419=
XM_011543676.1:c.16179G=	XP_011541978.1:p.Gln5393=
XM_011543677.1:c.13563G=	XP_011541979.1:p.Gln4521=
NM_032119.4:c.16260G= MANE Select	NP_115495.3:p.Gln5420=
XM_017009963.2:c.16281G=	XP_016865452.1:p.Gln5427=
XM_017009964.2:c.16278G=	XP_016865453.1:p.Gln5426=
XM_017009965.1:c.16278G=	XP_016865454.1:p.Gln5426=
XM_017009966.2:c.16200G=	XP_016865455.1:p.Gln5400=
XM_017009967.1:c.16185G=	XP_016865456.1:p.Gln5395=
XM_017009968.2:c.16101G=	XP_016865457.1:p.Gln5367=
XM_017009969.2:c.16281G=	XP_016865458.1:p.Gln5427=
XM_017009972.1:c.9399G=	XP_016865461.1:p.Gln3133=
XM_017009973.1:c.9378G=	XP_016865462.1:p.Gln3126=
NR_003149.2:n.16276G=