Canonical Allele Identifier: CA476881701

Gene: APOA5

Linked Data

• gnomAD v4: 11-116789964-C-A
• MyVariant Identifiers: chr11:g.116660680C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116789964C>A , CM000673.2:g.116789964C>A	GRCh38
NC_000011.9:g.116660680C>A , CM000673.1:g.116660680C>A	GRCh37
NC_000011.8:g.116165890C>A	NCBI36
NG_015894.1:g.7457G>T
NG_015894.2:g.7457G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000227665.9:c.*164G>T MANE Select	ENSP00000227665.4:n.*164G>T
ENST00000433069.2:c.*164G>T	ENSP00000399701.2:n.*164G>T
ENST00000227665.8:c.*164G>T	ENSP00000227665.4:n.*164G>T
ENST00000542499.5:c.*164G>T	ENSP00000445002.1:n.*164G>T
NM_001166598.1:c.*164G>T	NP_001160070.1:n.*164G>T
NM_052968.4:c.*164G>T	NP_443200.2:n.*164G>T
NM_001166598.2:c.*164G>T	NP_001160070.1:n.*164G>T
NM_001371904.1:c.*164G>T MANE Select	NP_001358833.1:n.*164G>T
NM_052968.5:c.*164G>T	NP_443200.2:n.*164G>T