Canonical Allele Identifier: CA382740556

Gene: APOA5

Linked Data

• MyVariant Identifiers: chr11:g.116661784C>G (hg19) ; chr11:g.116791068C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116791068C>G , CM000673.2:g.116791068C>G	GRCh38
NC_000011.9:g.116661784C>G , CM000673.1:g.116661784C>G	GRCh37
NC_000011.8:g.116166994C>G	NCBI36
NG_015894.1:g.6353G>C
NG_015894.2:g.6353G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227665.9:c.162-1G>C MANE Select	ENSP00000227665.4:n.162-1G>C
ENST00000433069.2:c.162-1G>C	ENSP00000399701.2:n.162-1G>C
ENST00000673688.1:c.245G>C	ENSP00000501141.1:p.Arg82Thr
ENST00000227665.8:c.162-1G>C	ENSP00000227665.4:n.162-1G>C
ENST00000433069.1:c.162-1G>C	ENSP00000399701.1:n.162-1G>C
ENST00000542499.5:c.162-1G>C	ENSP00000445002.1:n.162-1G>C
NM_001166598.1:c.162-1G>C	NP_001160070.1:n.162-1G>C
NM_052968.4:c.162-1G>C	NP_443200.2:n.162-1G>C
NM_001166598.2:c.162-1G>C	NP_001160070.1:n.162-1G>C
NM_001371904.1:c.162-1G>C MANE Select	NP_001358833.1:n.162-1G>C
NM_052968.5:c.162-1G>C	NP_443200.2:n.162-1G>C