Canonical Allele Identifier: CA382713855
Gene: APOA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116835849T>C , CM000673.2:g.116835849T>C GRCh38
NC_000011.9:g.116706565T>C , CM000673.1:g.116706565T>C GRCh37
NC_000011.8:g.116211775T>C NCBI36
NG_012021.1:g.6774A>G , LRG_767:g.6774A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000236850.5:c.763A>G MANE Select ENSP00000236850.3:p.Ser255Gly
ENST00000236850.4:c.763A>G ENSP00000236850.3:p.Ser255Gly
ENST00000359492.6:c.763A>G ENSP00000352471.2:p.Ser255Gly
ENST00000375320.5:c.763A>G ENSP00000364469.1:p.Ser255Gly
ENST00000375323.5:c.763A>G ENSP00000364472.1:p.Ser255Gly
ENST00000375329.6:c.697A>G ENSP00000364478.2:p.Ser233Gly
NM_000039.1:c.763A>G , LRG_767t1:c.763A>G NP_000030.1:p.Ser255Gly
XM_005271539.2:c.763A>G XP_005271596.1:p.Ser255Gly
XM_005271540.1:c.763A>G XP_005271597.1:p.Ser255Gly
NM_000039.2:c.763A>G NP_000030.1:p.Ser255Gly
NM_001318017.1:c.763A>G NP_001304946.1:p.Ser255Gly
NM_001318018.1:c.763A>G NP_001304947.1:p.Ser255Gly
NM_001318021.1:c.436A>G NP_001304950.1:p.Ser146Gly
NM_001318017.2:c.763A>G NP_001304946.1:p.Ser255Gly
NM_001318018.2:c.763A>G NP_001304947.1:p.Ser255Gly
NM_000039.3:c.763A>G MANE Select NP_000030.1:p.Ser255Gly