Canonical Allele Identifier: CA229336951
Gene: APOA5 HGNC NCBI

Linked Data

dbSNP Id: rs910507614
MyVariant Identifiers: chr11:g.116660702C>T (hg19) chr11:g.116789986C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116789986C>T , CM000673.2:g.116789986C>T GRCh38
NC_000011.9:g.116660702C>T , CM000673.1:g.116660702C>T GRCh37
NC_000011.8:g.116165912C>T NCBI36
NG_015894.1:g.7435G>A
NG_015894.2:g.7435G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000227665.9:c.*142G>A MANE Select ENSP00000227665.4:n.*142G>A
ENST00000433069.2:c.*142G>A ENSP00000399701.2:n.*142G>A
ENST00000227665.8:c.*142G>A ENSP00000227665.4:n.*142G>A
ENST00000542499.5:c.*142G>A ENSP00000445002.1:n.*142G>A
NM_001166598.1:c.*142G>A NP_001160070.1:n.*142G>A
NM_052968.4:c.*142G>A NP_443200.2:n.*142G>A
NM_001166598.2:c.*142G>A NP_001160070.1:n.*142G>A
NM_001371904.1:c.*142G>A MANE Select NP_001358833.1:n.*142G>A
NM_052968.5:c.*142G>A NP_443200.2:n.*142G>A
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