Canonical Allele Identifier: CA1562867553

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712387C= , CM000667.2:g.90712387C=	GRCh38
NC_000005.9:g.90008204C= , CM000667.1:g.90008204C=	GRCh37
NC_000005.8:g.90043960C=	NCBI36
NG_007083.1:g.158588C=
NG_007083.2:g.188044C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9143C= MANE Select	ENSP00000384582.2:p.Thr3048=
ENST00000639431.1:c.265+36178C=	ENSP00000491057.1:n.265+36178C=
ENST00000639473.1:n.4602C=
ENST00000640012.1:c.2950C=
ENST00000640374.1:n.2287C=
ENST00000640779.1:c.3872C=
ENST00000405460.6:c.9143C=	ENSP00000384582.2:p.Thr3048=
ENST00000509621.1:c.1840C=
NM_032119.3:c.9143C=	NP_115495.3:p.Thr3048=
NR_003149.1:n.9156C=
XM_011543675.1:c.9140C=	XP_011541977.1:p.Thr3047=
XM_011543676.1:c.9062C=	XP_011541978.1:p.Thr3021=
XM_011543677.1:c.6446C=	XP_011541979.1:p.Thr2149=
XM_011543678.1:c.9143C=	XP_011541980.1:p.Thr3048=
XM_011543679.1:c.9143C=	XP_011541981.1:p.Thr3048=
XR_948560.1:n.459G=
NM_032119.4:c.9143C= MANE Select	NP_115495.3:p.Thr3048=
XM_017009963.2:c.9164C=	XP_016865452.1:p.Thr3055=
XM_017009964.2:c.9161C=	XP_016865453.1:p.Thr3054=
XM_017009965.1:c.9161C=	XP_016865454.1:p.Thr3054=
XM_017009966.2:c.9083C=	XP_016865455.1:p.Thr3028=
XM_017009967.1:c.9068C=	XP_016865456.1:p.Thr3023=
XM_017009968.2:c.9164C=	XP_016865457.1:p.Thr3055=
XM_017009969.2:c.9164C=	XP_016865458.1:p.Thr3055=
XM_017009970.2:c.9164C=	XP_016865459.1:p.Thr3055=
XM_017009971.2:c.9164C=	XP_016865460.1:p.Thr3055=
XM_017009972.1:c.2282C=	XP_016865461.1:p.Thr761=
XM_017009973.1:c.2261C=	XP_016865462.1:p.Thr754=
XM_017009974.2:c.9164C=	XP_016865463.1:p.Thr3055=
NR_003149.2:n.9159C=