Canonical Allele Identifier: CA1562829367

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90627440T= , CM000667.2:g.90627440T=	GRCh38
NC_000005.9:g.89923257T= , CM000667.1:g.89923257T=	GRCh37
NC_000005.8:g.89959013T=	NCBI36
NG_007083.1:g.73641T=
NG_007083.2:g.103097T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.902T= MANE Select	ENSP00000384582.2:p.Val301=
ENST00000640083.1:n.607T=
ENST00000640109.1:n.998T=
ENST00000640281.1:n.961T=
ENST00000405460.6:c.902T=	ENSP00000384582.2:p.Val301=
NM_032119.3:c.902T=	NP_115495.3:p.Val301=
NR_003149.1:n.998T=
XM_011543675.1:c.902T=	XP_011541977.1:p.Val301=
XM_011543676.1:c.902T=	XP_011541978.1:p.Val301=
XM_011543678.1:c.902T=	XP_011541980.1:p.Val301=
XM_011543679.1:c.902T=	XP_011541981.1:p.Val301=
NM_032119.4:c.902T= MANE Select	NP_115495.3:p.Val301=
XM_017009963.2:c.902T=	XP_016865452.1:p.Val301=
XM_017009964.2:c.902T=	XP_016865453.1:p.Val301=
XM_017009965.1:c.899T=	XP_016865454.1:p.Val300=
XM_017009966.2:c.902T=	XP_016865455.1:p.Val301=
XM_017009967.1:c.806T=	XP_016865456.1:p.Val269=
XM_017009968.2:c.902T=	XP_016865457.1:p.Val301=
XM_017009969.2:c.902T=	XP_016865458.1:p.Val301=
XM_017009970.2:c.902T=	XP_016865459.1:p.Val301=
XM_017009971.2:c.902T=	XP_016865460.1:p.Val301=
XM_017009974.2:c.902T=	XP_016865463.1:p.Val301=
NR_003149.2:n.1001T=