Canonical Allele Identifier: CA2002762400

Gene: APOA1 APOA1-AS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116837100C= , CM000673.2:g.116837100C=	GRCh38
NC_000011.9:g.116707816C= , CM000673.1:g.116707816C=	GRCh37
NC_000011.8:g.116213026C=	NCBI36
NG_012021.1:g.5523G= , LRG_767:g.5523G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236850.5:c.101G= (APOA1) MANE Select	ENSP00000236850.3:p.Arg34=
ENST00000236850.4:c.101G= (APOA1)	ENSP00000236850.3:p.Arg34=
ENST00000359492.6:c.101G= (APOA1)	ENSP00000352471.2:p.Arg34=
ENST00000375320.5:c.101G= (APOA1)	ENSP00000364469.1:p.Arg34=
ENST00000375323.5:c.101G= (APOA1)	ENSP00000364472.1:p.Arg34=
ENST00000375329.6:c.134+245G= (APOA1)	ENSP00000364478.2:n.134+245G=
NM_000039.1:c.101G= , LRG_767t1:c.101G= (APOA1)	NP_000030.1:p.Arg34=
NR_126362.1:n.123+861C= (APOA1-AS)
XM_005271539.2:c.101G= (APOA1)	XP_005271596.1:p.Arg34=
XM_005271540.1:c.101G= (APOA1)	XP_005271597.1:p.Arg34=
NM_000039.2:c.101G= (APOA1)	NP_000030.1:p.Arg34=
NM_001318017.1:c.101G= (APOA1)	NP_001304946.1:p.Arg34=
NM_001318018.1:c.101G= (APOA1)	NP_001304947.1:p.Arg34=
NM_001318021.1:c.-227G= (APOA1)	NP_001304950.1:n.-227G=
NM_001318017.2:c.101G= (APOA1)	NP_001304946.1:p.Arg34=
NM_001318018.2:c.101G= (APOA1)	NP_001304947.1:p.Arg34=
NM_000039.3:c.101G= (APOA1) MANE Select	NP_000030.1:p.Arg34=