Canonical Allele Identifier: CA1562886231

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755164T= , CM000667.2:g.90755164T=	GRCh38
NC_000005.9:g.90050981T= , CM000667.1:g.90050981T=	GRCh37
NC_000005.8:g.90086737T=	NCBI36
NG_007083.1:g.201365T=
NG_007083.2:g.230821T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11559T= MANE Select	ENSP00000384582.2:p.His3853=
ENST00000425867.3:c.690T=	ENSP00000392618.3:p.His230=
ENST00000639431.1:c.265+78955T=	ENSP00000491057.1:n.265+78955T=
ENST00000640374.1:n.4703T=
ENST00000640464.1:n.1978T=
ENST00000405460.6:c.11559T=	ENSP00000384582.2:p.His3853=
ENST00000509621.1:c.4256T=
NM_032119.3:c.11559T=	NP_115495.3:p.His3853=
NR_003149.1:n.11572T=
XM_011543675.1:c.11556T=	XP_011541977.1:p.His3852=
XM_011543676.1:c.11478T=	XP_011541978.1:p.His3826=
XM_011543677.1:c.8862T=	XP_011541979.1:p.His2954=
XM_011543678.1:c.11559T=	XP_011541980.1:p.His3853=
NM_032119.4:c.11559T= MANE Select	NP_115495.3:p.His3853=
XM_017009963.2:c.11580T=	XP_016865452.1:p.His3860=
XM_017009964.2:c.11577T=	XP_016865453.1:p.His3859=
XM_017009965.1:c.11577T=	XP_016865454.1:p.His3859=
XM_017009966.2:c.11499T=	XP_016865455.1:p.His3833=
XM_017009967.1:c.11484T=	XP_016865456.1:p.His3828=
XM_017009968.2:c.11580T=	XP_016865457.1:p.His3860=
XM_017009969.2:c.11580T=	XP_016865458.1:p.His3860=
XM_017009970.2:c.11580T=	XP_016865459.1:p.His3860=
XM_017009971.2:c.11580T=	XP_016865460.1:p.His3860=
XM_017009972.1:c.4698T=	XP_016865461.1:p.His1566=
XM_017009973.1:c.4677T=	XP_016865462.1:p.His1559=
NR_003149.2:n.11575T=