Canonical Allele Identifier: CA1562886217

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755127C= , CM000667.2:g.90755127C=	GRCh38
NC_000005.9:g.90050944C= , CM000667.1:g.90050944C=	GRCh37
NC_000005.8:g.90086700C=	NCBI36
NG_007083.1:g.201328C=
NG_007083.2:g.230784C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11522C= MANE Select	ENSP00000384582.2:p.Thr3841=
ENST00000425867.3:c.653C=	ENSP00000392618.3:p.Thr218=
ENST00000639431.1:c.265+78918C=	ENSP00000491057.1:n.265+78918C=
ENST00000640374.1:n.4666C=
ENST00000640464.1:n.1941C=
ENST00000405460.6:c.11522C=	ENSP00000384582.2:p.Thr3841=
ENST00000509621.1:c.4219C=
NM_032119.3:c.11522C=	NP_115495.3:p.Thr3841=
NR_003149.1:n.11535C=
XM_011543675.1:c.11519C=	XP_011541977.1:p.Thr3840=
XM_011543676.1:c.11441C=	XP_011541978.1:p.Thr3814=
XM_011543677.1:c.8825C=	XP_011541979.1:p.Thr2942=
XM_011543678.1:c.11522C=	XP_011541980.1:p.Thr3841=
NM_032119.4:c.11522C= MANE Select	NP_115495.3:p.Thr3841=
XM_017009963.2:c.11543C=	XP_016865452.1:p.Thr3848=
XM_017009964.2:c.11540C=	XP_016865453.1:p.Thr3847=
XM_017009965.1:c.11540C=	XP_016865454.1:p.Thr3847=
XM_017009966.2:c.11462C=	XP_016865455.1:p.Thr3821=
XM_017009967.1:c.11447C=	XP_016865456.1:p.Thr3816=
XM_017009968.2:c.11543C=	XP_016865457.1:p.Thr3848=
XM_017009969.2:c.11543C=	XP_016865458.1:p.Thr3848=
XM_017009970.2:c.11543C=	XP_016865459.1:p.Thr3848=
XM_017009971.2:c.11543C=	XP_016865460.1:p.Thr3848=
XM_017009972.1:c.4661C=	XP_016865461.1:p.Thr1554=
XM_017009973.1:c.4640C=	XP_016865462.1:p.Thr1547=
NR_003149.2:n.11538C=