Canonical Allele Identifier: CA1562889826

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90763257C= , CM000667.2:g.90763257C=	GRCh38
NC_000005.9:g.90059074C= , CM000667.1:g.90059074C=	GRCh37
NC_000005.8:g.90094830C=	NCBI36
NG_007083.1:g.209458C=
NG_007083.2:g.238914C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.12121-48C= MANE Select	ENSP00000384582.2:n.12121-48C=
ENST00000425867.3:c.1075-48C=	ENSP00000392618.3:n.1075-48C=
ENST00000639431.1:c.265+87048C=	ENSP00000491057.1:n.265+87048C=
ENST00000640464.1:n.2540-48C=
ENST00000640729.1:n.650C=
ENST00000405460.6:c.12121-48C=	ENSP00000384582.2:n.12121-48C=
NM_032119.3:c.12121-48C=	NP_115495.3:n.12121-48C=
NR_003149.1:n.12134-48C=
XM_011543675.1:c.12118-48C=	XP_011541977.1:n.12118-48C=
XM_011543676.1:c.12040-48C=	XP_011541978.1:n.12040-48C=
XM_011543677.1:c.9424-48C=	XP_011541979.1:n.9424-48C=
XM_011543678.1:c.12121-48C=	XP_011541980.1:n.12121-48C=
NM_032119.4:c.12121-48C= MANE Select	NP_115495.3:n.12121-48C=
XM_017009963.2:c.12142-48C=	XP_016865452.1:n.12142-48C=
XM_017009964.2:c.12139-48C=	XP_016865453.1:n.12139-48C=
XM_017009965.1:c.12139-48C=	XP_016865454.1:n.12139-48C=
XM_017009966.2:c.12061-48C=	XP_016865455.1:n.12061-48C=
XM_017009967.1:c.12046-48C=	XP_016865456.1:n.12046-48C=
XM_017009968.2:c.12142-48C=	XP_016865457.1:n.12142-48C=
XM_017009969.2:c.12142-48C=	XP_016865458.1:n.12142-48C=
XM_017009970.2:c.12142-48C=	XP_016865459.1:n.12142-48C=
XM_017009971.2:c.12142-48C=	XP_016865460.1:n.12142-48C=
XM_017009972.1:c.5260-48C=	XP_016865461.1:n.5260-48C=
XM_017009973.1:c.5239-48C=	XP_016865462.1:n.5239-48C=
NR_003149.2:n.12137-48C=