Canonical Allele Identifier: CA672155255

Gene: APOA5

Linked Data

• dbSNP Id: rs1418839136
• gnomAD v4: 11-116789976-G-A
• MyVariant Identifiers: chr11:g.116660692G>A (hg19) ; chr11:g.116789976G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116789976G>A , CM000673.2:g.116789976G>A	GRCh38
NC_000011.9:g.116660692G>A , CM000673.1:g.116660692G>A	GRCh37
NC_000011.8:g.116165902G>A	NCBI36
NG_015894.1:g.7445C>T
NG_015894.2:g.7445C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000227665.9:c.*152C>T MANE Select	ENSP00000227665.4:n.*152C>T
ENST00000433069.2:c.*152C>T	ENSP00000399701.2:n.*152C>T
ENST00000227665.8:c.*152C>T	ENSP00000227665.4:n.*152C>T
ENST00000542499.5:c.*152C>T	ENSP00000445002.1:n.*152C>T
NM_001166598.1:c.*152C>T	NP_001160070.1:n.*152C>T
NM_052968.4:c.*152C>T	NP_443200.2:n.*152C>T
NM_001166598.2:c.*152C>T	NP_001160070.1:n.*152C>T
NM_001371904.1:c.*152C>T MANE Select	NP_001358833.1:n.*152C>T
NM_052968.5:c.*152C>T	NP_443200.2:n.*152C>T