Canonical Allele Identifier: CA2002761925

Gene: APOA1 APOA1-AS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116836151G= , CM000673.2:g.116836151G=	GRCh38
NC_000011.9:g.116706867G= , CM000673.1:g.116706867G=	GRCh37
NC_000011.8:g.116212077G=	NCBI36
NG_012021.1:g.6472C= , LRG_767:g.6472C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236850.5:c.461C= (APOA1) MANE Select	ENSP00000236850.3:p.Ala154=
ENST00000236850.4:c.461C= (APOA1)	ENSP00000236850.3:p.Ala154=
ENST00000359492.6:c.461C= (APOA1)	ENSP00000352471.2:p.Ala154=
ENST00000375320.5:c.461C= (APOA1)	ENSP00000364469.1:p.Ala154=
ENST00000375323.5:c.461C= (APOA1)	ENSP00000364472.1:p.Ala154=
ENST00000375329.6:c.395C= (APOA1)	ENSP00000364478.2:p.Ala132=
NM_000039.1:c.461C= , LRG_767t1:c.461C= (APOA1)	NP_000030.1:p.Ala154=
NR_126362.1:n.35G= (APOA1-AS)
XM_005271539.2:c.461C= (APOA1)	XP_005271596.1:p.Ala154=
XM_005271540.1:c.461C= (APOA1)	XP_005271597.1:p.Ala154=
NM_000039.2:c.461C= (APOA1)	NP_000030.1:p.Ala154=
NM_001318017.1:c.461C= (APOA1)	NP_001304946.1:p.Ala154=
NM_001318018.1:c.461C= (APOA1)	NP_001304947.1:p.Ala154=
NM_001318021.1:c.134C= (APOA1)	NP_001304950.1:p.Ala45=
NM_001318017.2:c.461C= (APOA1)	NP_001304946.1:p.Ala154=
NM_001318018.2:c.461C= (APOA1)	NP_001304947.1:p.Ala154=
NM_000039.3:c.461C= (APOA1) MANE Select	NP_000030.1:p.Ala154=