Canonical Allele Identifier: CA445416127

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90041507T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745690T>C , CM000667.2:g.90745690T>C	GRCh38
NC_000005.9:g.90041507T>C , CM000667.1:g.90041507T>C	GRCh37
NC_000005.8:g.90077263T>C	NCBI36
NG_007083.1:g.191891T>C
NG_007083.2:g.221347T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10869T>C MANE Select	ENSP00000384582.2:p.Val3623=
ENST00000639431.1:c.265+69481T>C	ENSP00000491057.1:n.265+69481T>C
ENST00000640374.1:n.4013T>C
ENST00000640464.1:n.1288T>C
ENST00000405460.6:c.10869T>C	ENSP00000384582.2:p.Val3623=
ENST00000509621.1:c.3566T>C
NM_032119.3:c.10869T>C	NP_115495.3:p.Val3623=
NR_003149.1:n.10882T>C
XM_011543675.1:c.10866T>C	XP_011541977.1:p.Val3622=
XM_011543676.1:c.10788T>C	XP_011541978.1:p.Val3596=
XM_011543677.1:c.8172T>C	XP_011541979.1:p.Val2724=
XM_011543678.1:c.10869T>C	XP_011541980.1:p.Val3623=
NM_032119.4:c.10869T>C MANE Select	NP_115495.3:p.Val3623=
XM_017009963.2:c.10890T>C	XP_016865452.1:p.Val3630=
XM_017009964.2:c.10887T>C	XP_016865453.1:p.Val3629=
XM_017009965.1:c.10887T>C	XP_016865454.1:p.Val3629=
XM_017009966.2:c.10809T>C	XP_016865455.1:p.Val3603=
XM_017009967.1:c.10794T>C	XP_016865456.1:p.Val3598=
XM_017009968.2:c.10890T>C	XP_016865457.1:p.Val3630=
XM_017009969.2:c.10890T>C	XP_016865458.1:p.Val3630=
XM_017009970.2:c.10890T>C	XP_016865459.1:p.Val3630=
XM_017009971.2:c.10890T>C	XP_016865460.1:p.Val3630=
XM_017009972.1:c.4008T>C	XP_016865461.1:p.Val1336=
XM_017009973.1:c.3987T>C	XP_016865462.1:p.Val1329=
NR_003149.2:n.10885T>C