Canonical Allele Identifier: CA1562918262

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823479C= , CM000667.2:g.90823479C=	GRCh38
NC_000005.9:g.90119296C= , CM000667.1:g.90119296C=	GRCh37
NC_000005.8:g.90155052C=	NCBI36
NG_007083.1:g.269680C=
NG_007083.2:g.299136C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16251C= MANE Select	ENSP00000384582.2:p.Val5417=
ENST00000425867.3:c.5205C=	ENSP00000392618.3:p.Val1735=
ENST00000638510.1:n.3518C=
ENST00000639431.1:c.265+147270C=	ENSP00000491057.1:n.265+147270C=
ENST00000640061.1:n.128+1297C=
ENST00000640407.1:c.2661C=	ENSP00000491425.1:p.Val887=
ENST00000405460.6:c.16251C=	ENSP00000384582.2:p.Val5417=
ENST00000425867.2:c.3234C=	ENSP00000392618.2:p.Val1078=
NM_032119.3:c.16251C=	NP_115495.3:p.Val5417=
NR_003149.1:n.16264C=
XM_011543675.1:c.16248C=	XP_011541977.1:p.Val5416=
XM_011543676.1:c.16170C=	XP_011541978.1:p.Val5390=
XM_011543677.1:c.13554C=	XP_011541979.1:p.Val4518=
NM_032119.4:c.16251C= MANE Select	NP_115495.3:p.Val5417=
XM_017009963.2:c.16272C=	XP_016865452.1:p.Val5424=
XM_017009964.2:c.16269C=	XP_016865453.1:p.Val5423=
XM_017009965.1:c.16269C=	XP_016865454.1:p.Val5423=
XM_017009966.2:c.16191C=	XP_016865455.1:p.Val5397=
XM_017009967.1:c.16176C=	XP_016865456.1:p.Val5392=
XM_017009968.2:c.16092C=	XP_016865457.1:p.Val5364=
XM_017009969.2:c.16272C=	XP_016865458.1:p.Val5424=
XM_017009972.1:c.9390C=	XP_016865461.1:p.Val3130=
XM_017009973.1:c.9369C=	XP_016865462.1:p.Val3123=
NR_003149.2:n.16267C=