Canonical Allele Identifier: CA672157476

Gene: APOA5

Linked Data

• dbSNP Id: rs1199543090
• gnomAD v4: 11-116791090-A-G
• MyVariant Identifiers: chr11:g.116661806A>G (hg19) ; chr11:g.116791090A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116791090A>G , CM000673.2:g.116791090A>G	GRCh38
NC_000011.9:g.116661806A>G , CM000673.1:g.116661806A>G	GRCh37
NC_000011.8:g.116167016A>G	NCBI36
NG_015894.1:g.6331T>C
NG_015894.2:g.6331T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227665.9:c.162-23T>C MANE Select	ENSP00000227665.4:n.162-23T>C
ENST00000433069.2:c.162-23T>C	ENSP00000399701.2:n.162-23T>C
ENST00000673688.1:c.223T>C	ENSP00000501141.1:p.Trp75Arg
ENST00000227665.8:c.162-23T>C	ENSP00000227665.4:n.162-23T>C
ENST00000433069.1:c.162-23T>C	ENSP00000399701.1:n.162-23T>C
ENST00000542499.5:c.162-23T>C	ENSP00000445002.1:n.162-23T>C
NM_001166598.1:c.162-23T>C	NP_001160070.1:n.162-23T>C
NM_052968.4:c.162-23T>C	NP_443200.2:n.162-23T>C
NM_001166598.2:c.162-23T>C	NP_001160070.1:n.162-23T>C
NM_001371904.1:c.162-23T>C MANE Select	NP_001358833.1:n.162-23T>C
NM_052968.5:c.162-23T>C	NP_443200.2:n.162-23T>C