Canonical Allele Identifier: CA445407027
Gene: ADGRV1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.90059253T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90763436T>A , CM000667.2:g.90763436T>A GRCh38
NC_000005.9:g.90059253T>A , CM000667.1:g.90059253T>A GRCh37
NC_000005.8:g.90095009T>A NCBI36
NG_007083.1:g.209637T>A
NG_007083.2:g.239093T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.12252T>A MANE Select ENSP00000384582.2:p.Leu4084=
ENST00000425867.3:c.1206T>A ENSP00000392618.3:p.Leu402=
ENST00000639431.1:c.265+87227T>A ENSP00000491057.1:n.265+87227T>A
ENST00000640464.1:n.2671T>A
ENST00000640729.1:n.829T>A
ENST00000405460.6:c.12252T>A ENSP00000384582.2:p.Leu4084=
NM_032119.3:c.12252T>A NP_115495.3:p.Leu4084=
NR_003149.1:n.12265T>A
XM_011543675.1:c.12249T>A XP_011541977.1:p.Leu4083=
XM_011543676.1:c.12171T>A XP_011541978.1:p.Leu4057=
XM_011543677.1:c.9555T>A XP_011541979.1:p.Leu3185=
XM_011543678.1:c.12252T>A XP_011541980.1:p.Leu4084=
NM_032119.4:c.12252T>A MANE Select NP_115495.3:p.Leu4084=
XM_017009963.2:c.12273T>A XP_016865452.1:p.Leu4091=
XM_017009964.2:c.12270T>A XP_016865453.1:p.Leu4090=
XM_017009965.1:c.12270T>A XP_016865454.1:p.Leu4090=
XM_017009966.2:c.12192T>A XP_016865455.1:p.Leu4064=
XM_017009967.1:c.12177T>A XP_016865456.1:p.Leu4059=
XM_017009968.2:c.12273T>A XP_016865457.1:p.Leu4091=
XM_017009969.2:c.12273T>A XP_016865458.1:p.Leu4091=
XM_017009970.2:c.12273T>A XP_016865459.1:p.Leu4091=
XM_017009971.2:c.12273T>A XP_016865460.1:p.Leu4091=
XM_017009972.1:c.5391T>A XP_016865461.1:p.Leu1797=
XM_017009973.1:c.5370T>A XP_016865462.1:p.Leu1790=
NR_003149.2:n.12268T>A