Canonical Allele Identifier: CA445404233

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050990T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755173T>A , CM000667.2:g.90755173T>A	GRCh38
NC_000005.9:g.90050990T>A , CM000667.1:g.90050990T>A	GRCh37
NC_000005.8:g.90086746T>A	NCBI36
NG_007083.1:g.201374T>A
NG_007083.2:g.230830T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.11568T>A MANE Select	ENSP00000384582.2:p.Val3856=
ENST00000425867.3:c.699T>A	ENSP00000392618.3:p.Val233=
ENST00000639431.1:c.265+78964T>A	ENSP00000491057.1:n.265+78964T>A
ENST00000640374.1:n.4712T>A
ENST00000640464.1:n.1987T>A
ENST00000405460.6:c.11568T>A	ENSP00000384582.2:p.Val3856=
ENST00000509621.1:c.4265T>A
NM_032119.3:c.11568T>A	NP_115495.3:p.Val3856=
NR_003149.1:n.11581T>A
XM_011543675.1:c.11565T>A	XP_011541977.1:p.Val3855=
XM_011543676.1:c.11487T>A	XP_011541978.1:p.Val3829=
XM_011543677.1:c.8871T>A	XP_011541979.1:p.Val2957=
XM_011543678.1:c.11568T>A	XP_011541980.1:p.Val3856=
NM_032119.4:c.11568T>A MANE Select	NP_115495.3:p.Val3856=
XM_017009963.2:c.11589T>A	XP_016865452.1:p.Val3863=
XM_017009964.2:c.11586T>A	XP_016865453.1:p.Val3862=
XM_017009965.1:c.11586T>A	XP_016865454.1:p.Val3862=
XM_017009966.2:c.11508T>A	XP_016865455.1:p.Val3836=
XM_017009967.1:c.11493T>A	XP_016865456.1:p.Val3831=
XM_017009968.2:c.11589T>A	XP_016865457.1:p.Val3863=
XM_017009969.2:c.11589T>A	XP_016865458.1:p.Val3863=
XM_017009970.2:c.11589T>A	XP_016865459.1:p.Val3863=
XM_017009971.2:c.11589T>A	XP_016865460.1:p.Val3863=
XM_017009972.1:c.4707T>A	XP_016865461.1:p.Val1569=
XM_017009973.1:c.4686T>A	XP_016865462.1:p.Val1562=
NR_003149.2:n.11584T>A