Canonical Allele Identifier: CA6289129

Gene: APOA5

Linked Data

• dbSNP Id: rs762054961
• ExAC: 11:116661859 ACTGATCCTCTGGGGGAAC / A
• MyVariant Identifiers: chr11:g.116661860_116661877del (hg19) ; chr11:g.116791144_116791161del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116791145_116791162del , CM000673.2:g.116791145_116791162del	GRCh38
NC_000011.9:g.116661861_116661878del , CM000673.1:g.116661861_116661878del	GRCh37
NC_000011.8:g.116167071_116167088del	NCBI36
NG_015894.1:g.6260_6277del
NG_015894.2:g.6260_6277del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227665.9:c.162-94_162-77del MANE Select	ENSP00000227665.4:n.162-94_162-77del
ENST00000433069.2:c.162-94_162-77del	ENSP00000399701.2:n.162-94_162-77del
ENST00000673688.1:c.162-10_169del
ENST00000227665.8:c.162-94_162-77del	ENSP00000227665.4:n.162-94_162-77del
ENST00000433069.1:c.162-94_162-77del	ENSP00000399701.1:n.162-94_162-77del
ENST00000542499.5:c.162-94_162-77del	ENSP00000445002.1:n.162-94_162-77del
NM_001166598.1:c.162-94_162-77del	NP_001160070.1:n.162-94_162-77del
NM_052968.4:c.162-94_162-77del	NP_443200.2:n.162-94_162-77del
NM_001166598.2:c.162-94_162-77del	NP_001160070.1:n.162-94_162-77del
NM_001371904.1:c.162-94_162-77del MANE Select	NP_001358833.1:n.162-94_162-77del
NM_052968.5:c.162-94_162-77del	NP_443200.2:n.162-94_162-77del