Canonical Allele Identifier: CA1562825023

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90617835A= , CM000667.2:g.90617835A=	GRCh38
NC_000005.9:g.89913652A= , CM000667.1:g.89913652A=	GRCh37
NC_000005.8:g.89949408A=	NCBI36
NG_007083.1:g.64036A=
NG_007083.2:g.93492A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.239A= MANE Select	ENSP00000384582.2:p.Asp80=
ENST00000638316.1:n.449A=
ENST00000638638.1:n.646A=
ENST00000640109.1:n.335A=
ENST00000640281.1:n.298A=
ENST00000405460.6:c.239A=	ENSP00000384582.2:p.Asp80=
ENST00000508842.5:c.251A=	ENSP00000425936.1:p.Asp84=
NM_032119.3:c.239A=	NP_115495.3:p.Asp80=
NR_003149.1:n.335A=
XM_011543675.1:c.239A=	XP_011541977.1:p.Asp80=
XM_011543676.1:c.239A=	XP_011541978.1:p.Asp80=
XM_011543678.1:c.239A=	XP_011541980.1:p.Asp80=
XM_011543679.1:c.239A=	XP_011541981.1:p.Asp80=
NM_032119.4:c.239A= MANE Select	NP_115495.3:p.Asp80=
XM_017009963.2:c.239A=	XP_016865452.1:p.Asp80=
XM_017009964.2:c.239A=	XP_016865453.1:p.Asp80=
XM_017009965.1:c.236A=	XP_016865454.1:p.Asp79=
XM_017009966.2:c.239A=	XP_016865455.1:p.Asp80=
XM_017009967.1:c.239A=	XP_016865456.1:p.Asp80=
XM_017009968.2:c.239A=	XP_016865457.1:p.Asp80=
XM_017009969.2:c.239A=	XP_016865458.1:p.Asp80=
XM_017009970.2:c.239A=	XP_016865459.1:p.Asp80=
XM_017009971.2:c.239A=	XP_016865460.1:p.Asp80=
XM_017009974.2:c.239A=	XP_016865463.1:p.Asp80=
NR_003149.2:n.338A=