Canonical Allele Identifier: CA477047892

Gene: APOA5

Linked Data

• MyVariant Identifiers: chr11:g.116661657C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116790941C>G , CM000673.2:g.116790941C>G	GRCh38
NC_000011.9:g.116661657C>G , CM000673.1:g.116661657C>G	GRCh37
NC_000011.8:g.116166867C>G	NCBI36
NG_015894.1:g.6480G>C
NG_015894.2:g.6480G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000227665.9:c.288G>C MANE Select	ENSP00000227665.4:p.Leu96=
ENST00000433069.2:c.288G>C	ENSP00000399701.2:p.Leu96=
ENST00000673688.1:c.372G>C	ENSP00000501141.1:p.Leu124=
ENST00000227665.8:c.288G>C	ENSP00000227665.4:p.Leu96=
ENST00000433069.1:c.288G>C	ENSP00000399701.1:p.Leu96=
ENST00000542499.5:c.288G>C	ENSP00000445002.1:p.Leu96=
NM_001166598.1:c.288G>C	NP_001160070.1:p.Leu96=
NM_052968.4:c.288G>C	NP_443200.2:p.Leu96=
NM_001166598.2:c.288G>C	NP_001160070.1:p.Leu96=
NM_001371904.1:c.288G>C MANE Select	NP_001358833.1:p.Leu96=
NM_052968.5:c.288G>C	NP_443200.2:p.Leu96=