Canonical Allele Identifier: CA1562829378

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90627461C= , CM000667.2:g.90627461C=	GRCh38
NC_000005.9:g.89923278C= , CM000667.1:g.89923278C=	GRCh37
NC_000005.8:g.89959034C=	NCBI36
NG_007083.1:g.73662C=
NG_007083.2:g.103118C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.923C= MANE Select	ENSP00000384582.2:p.Thr308=
ENST00000640083.1:n.628C=
ENST00000640109.1:n.1019C=
ENST00000640281.1:n.982C=
ENST00000405460.6:c.923C=	ENSP00000384582.2:p.Thr308=
NM_032119.3:c.923C=	NP_115495.3:p.Thr308=
NR_003149.1:n.1019C=
XM_011543675.1:c.923C=	XP_011541977.1:p.Thr308=
XM_011543676.1:c.923C=	XP_011541978.1:p.Thr308=
XM_011543678.1:c.923C=	XP_011541980.1:p.Thr308=
XM_011543679.1:c.923C=	XP_011541981.1:p.Thr308=
NM_032119.4:c.923C= MANE Select	NP_115495.3:p.Thr308=
XM_017009963.2:c.923C=	XP_016865452.1:p.Thr308=
XM_017009964.2:c.923C=	XP_016865453.1:p.Thr308=
XM_017009965.1:c.920C=	XP_016865454.1:p.Thr307=
XM_017009966.2:c.923C=	XP_016865455.1:p.Thr308=
XM_017009967.1:c.827C=	XP_016865456.1:p.Thr276=
XM_017009968.2:c.923C=	XP_016865457.1:p.Thr308=
XM_017009969.2:c.923C=	XP_016865458.1:p.Thr308=
XM_017009970.2:c.923C=	XP_016865459.1:p.Thr308=
XM_017009971.2:c.923C=	XP_016865460.1:p.Thr308=
XM_017009974.2:c.923C=	XP_016865463.1:p.Thr308=
NR_003149.2:n.1022C=