Canonical Allele Identifier: CA229337152

Gene: APOA5

Linked Data

• dbSNP Id: rs61743807
• MyVariant Identifiers: chr11:g.116660945C>T (hg19) ; chr11:g.116790229C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116790229C>T , CM000673.2:g.116790229C>T	GRCh38
NC_000011.9:g.116660945C>T , CM000673.1:g.116660945C>T	GRCh37
NC_000011.8:g.116166155C>T	NCBI36
NG_015894.1:g.7192G>A
NG_015894.2:g.7192G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227665.9:c.1000G>A MANE Select	ENSP00000227665.4:p.Gly334Ser
ENST00000433069.2:c.1000G>A	ENSP00000399701.2:p.Gly334Ser
ENST00000673688.1:c.1084G>A	ENSP00000501141.1:p.Gly362Ser
ENST00000227665.8:c.1000G>A	ENSP00000227665.4:p.Gly334Ser
ENST00000542499.5:c.1000G>A	ENSP00000445002.1:p.Gly334Ser
NM_001166598.1:c.1000G>A	NP_001160070.1:p.Gly334Ser
NM_052968.4:c.1000G>A	NP_443200.2:p.Gly334Ser
NM_001166598.2:c.1000G>A	NP_001160070.1:p.Gly334Ser
NM_001371904.1:c.1000G>A MANE Select	NP_001358833.1:p.Gly334Ser
NM_052968.5:c.1000G>A	NP_443200.2:p.Gly334Ser