Canonical Allele Identifier: CA382737836

Gene: APOA5

Linked Data

• dbSNP Id: rs1414641825
• gnomAD v3: 11-116790621-C-G
• gnomAD v4: 11-116790621-C-G
• MyVariant Identifiers: chr11:g.116661337C>G (hg19) ; chr11:g.116790621C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116790621C>G , CM000673.2:g.116790621C>G	GRCh38
NC_000011.9:g.116661337C>G , CM000673.1:g.116661337C>G	GRCh37
NC_000011.8:g.116166547C>G	NCBI36
NG_015894.1:g.6800G>C
NG_015894.2:g.6800G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227665.9:c.608G>C MANE Select	ENSP00000227665.4:p.Gly203Ala
ENST00000433069.2:c.608G>C	ENSP00000399701.2:p.Gly203Ala
ENST00000673688.1:c.692G>C	ENSP00000501141.1:p.Gly231Ala
ENST00000227665.8:c.608G>C	ENSP00000227665.4:p.Gly203Ala
ENST00000542499.5:c.608G>C	ENSP00000445002.1:p.Gly203Ala
NM_001166598.1:c.608G>C	NP_001160070.1:p.Gly203Ala
NM_052968.4:c.608G>C	NP_443200.2:p.Gly203Ala
NM_001166598.2:c.608G>C	NP_001160070.1:p.Gly203Ala
NM_001371904.1:c.608G>C MANE Select	NP_001358833.1:p.Gly203Ala
NM_052968.5:c.608G>C	NP_443200.2:p.Gly203Ala