Canonical Allele Identifier: CA601831099

Gene: APOA5

Linked Data

• dbSNP Id: rs1356190082
• gnomAD v2: 11-116660696-C-T
• gnomAD v3: 11-116789980-C-T
• gnomAD v4: 11-116789980-C-T
• MyVariant Identifiers: chr11:g.116660696C>T (hg19) ; chr11:g.116789980C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116789980C>T , CM000673.2:g.116789980C>T	GRCh38
NC_000011.9:g.116660696C>T , CM000673.1:g.116660696C>T	GRCh37
NC_000011.8:g.116165906C>T	NCBI36
NG_015894.1:g.7441G>A
NG_015894.2:g.7441G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000227665.9:c.*148G>A MANE Select	ENSP00000227665.4:n.*148G>A
ENST00000433069.2:c.*148G>A	ENSP00000399701.2:n.*148G>A
ENST00000227665.8:c.*148G>A	ENSP00000227665.4:n.*148G>A
ENST00000542499.5:c.*148G>A	ENSP00000445002.1:n.*148G>A
NM_001166598.1:c.*148G>A	NP_001160070.1:n.*148G>A
NM_052968.4:c.*148G>A	NP_443200.2:n.*148G>A
NM_001166598.2:c.*148G>A	NP_001160070.1:n.*148G>A
NM_001371904.1:c.*148G>A MANE Select	NP_001358833.1:n.*148G>A
NM_052968.5:c.*148G>A	NP_443200.2:n.*148G>A