Canonical Allele Identifier: CA601831223
Gene: APOA5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.116661862G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116791146G>A , CM000673.2:g.116791146G>A GRCh38
NC_000011.9:g.116661862G>A , CM000673.1:g.116661862G>A GRCh37
NC_000011.8:g.116167072G>A NCBI36
NG_015894.1:g.6275C>T
NG_015894.2:g.6275C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000227665.9:c.162-79C>T MANE Select ENSP00000227665.4:n.162-79C>T
ENST00000433069.2:c.162-79C>T ENSP00000399701.2:n.162-79C>T
ENST00000673688.1:c.167C>T ENSP00000501141.1:p.Ser56Leu
ENST00000227665.8:c.162-79C>T ENSP00000227665.4:n.162-79C>T
ENST00000433069.1:c.162-79C>T ENSP00000399701.1:n.162-79C>T
ENST00000542499.5:c.162-79C>T ENSP00000445002.1:n.162-79C>T
NM_001166598.1:c.162-79C>T NP_001160070.1:n.162-79C>T
NM_052968.4:c.162-79C>T NP_443200.2:n.162-79C>T
NM_001166598.2:c.162-79C>T NP_001160070.1:n.162-79C>T
NM_001371904.1:c.162-79C>T MANE Select NP_001358833.1:n.162-79C>T
NM_052968.5:c.162-79C>T NP_443200.2:n.162-79C>T