Canonical Allele Identifier: CA2616085439
Gene: APOA5 HGNC NCBI

Linked Data

gnomAD v4: 11-116789979-A-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116789979A>T , CM000673.2:g.116789979A>T GRCh38
NC_000011.9:g.116660695A>T , CM000673.1:g.116660695A>T GRCh37
NC_000011.8:g.116165905A>T NCBI36
NG_015894.1:g.7442T>A
NG_015894.2:g.7442T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000227665.9:c.*149T>A MANE Select ENSP00000227665.4:n.*149T>A
ENST00000433069.2:c.*149T>A ENSP00000399701.2:n.*149T>A
ENST00000227665.8:c.*149T>A ENSP00000227665.4:n.*149T>A
ENST00000542499.5:c.*149T>A ENSP00000445002.1:n.*149T>A
NM_001166598.1:c.*149T>A NP_001160070.1:n.*149T>A
NM_052968.4:c.*149T>A NP_443200.2:n.*149T>A
NM_001166598.2:c.*149T>A NP_001160070.1:n.*149T>A
NM_001371904.1:c.*149T>A MANE Select NP_001358833.1:n.*149T>A
NM_052968.5:c.*149T>A NP_443200.2:n.*149T>A
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