Canonical Allele Identifier: CA445404238

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050993C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755176C>T , CM000667.2:g.90755176C>T	GRCh38
NC_000005.9:g.90050993C>T , CM000667.1:g.90050993C>T	GRCh37
NC_000005.8:g.90086749C>T	NCBI36
NG_007083.1:g.201377C>T
NG_007083.2:g.230833C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.11571C>T MANE Select	ENSP00000384582.2:p.Ser3857=
ENST00000425867.3:c.702C>T	ENSP00000392618.3:p.Ser234=
ENST00000639431.1:c.265+78967C>T	ENSP00000491057.1:n.265+78967C>T
ENST00000640374.1:n.4715C>T
ENST00000640464.1:n.1990C>T
ENST00000405460.6:c.11571C>T	ENSP00000384582.2:p.Ser3857=
ENST00000509621.1:c.4268C>T
NM_032119.3:c.11571C>T	NP_115495.3:p.Ser3857=
NR_003149.1:n.11584C>T
XM_011543675.1:c.11568C>T	XP_011541977.1:p.Ser3856=
XM_011543676.1:c.11490C>T	XP_011541978.1:p.Ser3830=
XM_011543677.1:c.8874C>T	XP_011541979.1:p.Ser2958=
XM_011543678.1:c.11571C>T	XP_011541980.1:p.Ser3857=
NM_032119.4:c.11571C>T MANE Select	NP_115495.3:p.Ser3857=
XM_017009963.2:c.11592C>T	XP_016865452.1:p.Ser3864=
XM_017009964.2:c.11589C>T	XP_016865453.1:p.Ser3863=
XM_017009965.1:c.11589C>T	XP_016865454.1:p.Ser3863=
XM_017009966.2:c.11511C>T	XP_016865455.1:p.Ser3837=
XM_017009967.1:c.11496C>T	XP_016865456.1:p.Ser3832=
XM_017009968.2:c.11592C>T	XP_016865457.1:p.Ser3864=
XM_017009969.2:c.11592C>T	XP_016865458.1:p.Ser3864=
XM_017009970.2:c.11592C>T	XP_016865459.1:p.Ser3864=
XM_017009971.2:c.11592C>T	XP_016865460.1:p.Ser3864=
XM_017009972.1:c.4710C>T	XP_016865461.1:p.Ser1570=
XM_017009973.1:c.4689C>T	XP_016865462.1:p.Ser1563=
NR_003149.2:n.11587C>T