Canonical Allele Identifier: CA2002761909
Gene: APOA1 HGNC NCBI
APOA1-AS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116836120C= , CM000673.2:g.116836120C= GRCh38
NC_000011.9:g.116706836C= , CM000673.1:g.116706836C= GRCh37
NC_000011.8:g.116212046C= NCBI36
NG_012021.1:g.6503G= , LRG_767:g.6503G=

Transcript Alleles

HGVS Amino-acid change
ENST00000236850.5:c.492G= (APOA1) MANE Select ENSP00000236850.3:p.Lys164=
ENST00000236850.4:c.492G= (APOA1) ENSP00000236850.3:p.Lys164=
ENST00000359492.6:c.492G= (APOA1) ENSP00000352471.2:p.Lys164=
ENST00000375320.5:c.492G= (APOA1) ENSP00000364469.1:p.Lys164=
ENST00000375323.5:c.492G= (APOA1) ENSP00000364472.1:p.Lys164=
ENST00000375329.6:c.426G= (APOA1) ENSP00000364478.2:p.Lys142=
NM_000039.1:c.492G= , LRG_767t1:c.492G= (APOA1) NP_000030.1:p.Lys164=
NR_126362.1:n.4C= (APOA1-AS)
XM_005271539.2:c.492G= (APOA1) XP_005271596.1:p.Lys164=
XM_005271540.1:c.492G= (APOA1) XP_005271597.1:p.Lys164=
NM_000039.2:c.492G= (APOA1) NP_000030.1:p.Lys164=
NM_001318017.1:c.492G= (APOA1) NP_001304946.1:p.Lys164=
NM_001318018.1:c.492G= (APOA1) NP_001304947.1:p.Lys164=
NM_001318021.1:c.165G= (APOA1) NP_001304950.1:p.Lys55=
NM_001318017.2:c.492G= (APOA1) NP_001304946.1:p.Lys164=
NM_001318018.2:c.492G= (APOA1) NP_001304947.1:p.Lys164=
NM_000039.3:c.492G= (APOA1) MANE Select NP_000030.1:p.Lys164=