Canonical Allele Identifier: CA1562911582

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90810900G= , CM000667.2:g.90810900G=	GRCh38
NC_000005.9:g.90106717G= , CM000667.1:g.90106717G=	GRCh37
NC_000005.8:g.90142473G=	NCBI36
NG_007083.1:g.257101G=
NG_007083.2:g.286557G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.15640G= MANE Select	ENSP00000384582.2:p.Val5214=
ENST00000425867.3:c.4594G=	ENSP00000392618.3:p.Val1532=
ENST00000638510.1:n.2907G=
ENST00000639431.1:c.265+134691G=	ENSP00000491057.1:n.265+134691G=
ENST00000640407.1:c.2050G=	ENSP00000491425.1:p.Val684=
ENST00000405460.6:c.15640G=	ENSP00000384582.2:p.Val5214=
ENST00000425867.2:c.2623G=	ENSP00000392618.2:p.Val875=
NM_032119.3:c.15640G=	NP_115495.3:p.Val5214=
NR_003149.1:n.15653G=
XM_011543675.1:c.15637G=	XP_011541977.1:p.Val5213=
XM_011543676.1:c.15559G=	XP_011541978.1:p.Val5187=
XM_011543677.1:c.12943G=	XP_011541979.1:p.Val4315=
NM_032119.4:c.15640G= MANE Select	NP_115495.3:p.Val5214=
XM_017009963.2:c.15661G=	XP_016865452.1:p.Val5221=
XM_017009964.2:c.15658G=	XP_016865453.1:p.Val5220=
XM_017009965.1:c.15658G=	XP_016865454.1:p.Val5220=
XM_017009966.2:c.15580G=	XP_016865455.1:p.Val5194=
XM_017009967.1:c.15565G=	XP_016865456.1:p.Val5189=
XM_017009968.2:c.15481G=	XP_016865457.1:p.Val5161=
XM_017009969.2:c.15661G=	XP_016865458.1:p.Val5221=
XM_017009972.1:c.8779G=	XP_016865461.1:p.Val2927=
XM_017009973.1:c.8758G=	XP_016865462.1:p.Val2920=
NR_003149.2:n.15656G=