Canonical Allele Identifier: CA2616085425
Gene: APOA5 HGNC NCBI

Linked Data

gnomAD v4: 11-116789975-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116789975G>T , CM000673.2:g.116789975G>T GRCh38
NC_000011.9:g.116660691G>T , CM000673.1:g.116660691G>T GRCh37
NC_000011.8:g.116165901G>T NCBI36
NG_015894.1:g.7446C>A
NG_015894.2:g.7446C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000227665.9:c.*153C>A MANE Select ENSP00000227665.4:n.*153C>A
ENST00000433069.2:c.*153C>A ENSP00000399701.2:n.*153C>A
ENST00000227665.8:c.*153C>A ENSP00000227665.4:n.*153C>A
ENST00000542499.5:c.*153C>A ENSP00000445002.1:n.*153C>A
NM_001166598.1:c.*153C>A NP_001160070.1:n.*153C>A
NM_052968.4:c.*153C>A NP_443200.2:n.*153C>A
NM_001166598.2:c.*153C>A NP_001160070.1:n.*153C>A
NM_001371904.1:c.*153C>A MANE Select NP_001358833.1:n.*153C>A
NM_052968.5:c.*153C>A NP_443200.2:n.*153C>A
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