Canonical Allele Identifier: CA382738425
Gene: APOA5 HGNC NCBI

Linked Data

dbSNP Id: rs2134203509

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116790798A>C , CM000673.2:g.116790798A>C GRCh38
NC_000011.9:g.116661514A>C , CM000673.1:g.116661514A>C GRCh37
NC_000011.8:g.116166724A>C NCBI36
NG_015894.1:g.6623T>G
NG_015894.2:g.6623T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000227665.9:c.431T>G MANE Select ENSP00000227665.4:p.Val144Gly
ENST00000433069.2:c.431T>G ENSP00000399701.2:p.Val144Gly
ENST00000673688.1:c.515T>G ENSP00000501141.1:p.Val172Gly
ENST00000227665.8:c.431T>G ENSP00000227665.4:p.Val144Gly
ENST00000433069.1:c.431T>G ENSP00000399701.1:p.Val144Gly
ENST00000542499.5:c.431T>G ENSP00000445002.1:p.Val144Gly
NM_001166598.1:c.431T>G NP_001160070.1:p.Val144Gly
NM_052968.4:c.431T>G NP_443200.2:p.Val144Gly
NM_001166598.2:c.431T>G NP_001160070.1:p.Val144Gly
NM_001371904.1:c.431T>G MANE Select NP_001358833.1:p.Val144Gly
NM_052968.5:c.431T>G NP_443200.2:p.Val144Gly