Canonical Allele Identifier: CA445403997

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050831T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755014T>C , CM000667.2:g.90755014T>C	GRCh38
NC_000005.9:g.90050831T>C , CM000667.1:g.90050831T>C	GRCh37
NC_000005.8:g.90086587T>C	NCBI36
NG_007083.1:g.201215T>C
NG_007083.2:g.230671T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11409T>C MANE Select	ENSP00000384582.2:p.Ala3803=
ENST00000425867.3:c.540T>C	ENSP00000392618.3:p.Ala180=
ENST00000639431.1:c.265+78805T>C	ENSP00000491057.1:n.265+78805T>C
ENST00000640374.1:n.4553T>C
ENST00000640464.1:n.1828T>C
ENST00000405460.6:c.11409T>C	ENSP00000384582.2:p.Ala3803=
ENST00000509621.1:c.4106T>C
NM_032119.3:c.11409T>C	NP_115495.3:p.Ala3803=
NR_003149.1:n.11422T>C
XM_011543675.1:c.11406T>C	XP_011541977.1:p.Ala3802=
XM_011543676.1:c.11328T>C	XP_011541978.1:p.Ala3776=
XM_011543677.1:c.8712T>C	XP_011541979.1:p.Ala2904=
XM_011543678.1:c.11409T>C	XP_011541980.1:p.Ala3803=
NM_032119.4:c.11409T>C MANE Select	NP_115495.3:p.Ala3803=
XM_017009963.2:c.11430T>C	XP_016865452.1:p.Ala3810=
XM_017009964.2:c.11427T>C	XP_016865453.1:p.Ala3809=
XM_017009965.1:c.11427T>C	XP_016865454.1:p.Ala3809=
XM_017009966.2:c.11349T>C	XP_016865455.1:p.Ala3783=
XM_017009967.1:c.11334T>C	XP_016865456.1:p.Ala3778=
XM_017009968.2:c.11430T>C	XP_016865457.1:p.Ala3810=
XM_017009969.2:c.11430T>C	XP_016865458.1:p.Ala3810=
XM_017009970.2:c.11430T>C	XP_016865459.1:p.Ala3810=
XM_017009971.2:c.11430T>C	XP_016865460.1:p.Ala3810=
XM_017009972.1:c.4548T>C	XP_016865461.1:p.Ala1516=
XM_017009973.1:c.4527T>C	XP_016865462.1:p.Ala1509=
NR_003149.2:n.11425T>C