Canonical Allele Identifier: CA1562918260

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823476C= , CM000667.2:g.90823476C=	GRCh38
NC_000005.9:g.90119293C= , CM000667.1:g.90119293C=	GRCh37
NC_000005.8:g.90155049C=	NCBI36
NG_007083.1:g.269677C=
NG_007083.2:g.299133C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.16248C= MANE Select	ENSP00000384582.2:p.Val5416=
ENST00000425867.3:c.5202C=	ENSP00000392618.3:p.Val1734=
ENST00000638510.1:n.3515C=
ENST00000639431.1:c.265+147267C=	ENSP00000491057.1:n.265+147267C=
ENST00000640061.1:n.128+1294C=
ENST00000640407.1:c.2658C=	ENSP00000491425.1:p.Val886=
ENST00000405460.6:c.16248C=	ENSP00000384582.2:p.Val5416=
ENST00000425867.2:c.3231C=	ENSP00000392618.2:p.Val1077=
NM_032119.3:c.16248C=	NP_115495.3:p.Val5416=
NR_003149.1:n.16261C=
XM_011543675.1:c.16245C=	XP_011541977.1:p.Val5415=
XM_011543676.1:c.16167C=	XP_011541978.1:p.Val5389=
XM_011543677.1:c.13551C=	XP_011541979.1:p.Val4517=
NM_032119.4:c.16248C= MANE Select	NP_115495.3:p.Val5416=
XM_017009963.2:c.16269C=	XP_016865452.1:p.Val5423=
XM_017009964.2:c.16266C=	XP_016865453.1:p.Val5422=
XM_017009965.1:c.16266C=	XP_016865454.1:p.Val5422=
XM_017009966.2:c.16188C=	XP_016865455.1:p.Val5396=
XM_017009967.1:c.16173C=	XP_016865456.1:p.Val5391=
XM_017009968.2:c.16089C=	XP_016865457.1:p.Val5363=
XM_017009969.2:c.16269C=	XP_016865458.1:p.Val5423=
XM_017009972.1:c.9387C=	XP_016865461.1:p.Val3129=
XM_017009973.1:c.9366C=	XP_016865462.1:p.Val3122=
NR_003149.2:n.16264C=