Canonical Allele Identifier: CA2002761845

Gene: APOA1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116836021G= , CM000673.2:g.116836021G=	GRCh38
NC_000011.9:g.116706737G= , CM000673.1:g.116706737G=	GRCh37
NC_000011.8:g.116211947G=	NCBI36
NG_012021.1:g.6602C= , LRG_767:g.6602C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236850.5:c.591C= MANE Select	ENSP00000236850.3:p.Arg197=
ENST00000236850.4:c.591C=	ENSP00000236850.3:p.Arg197=
ENST00000359492.6:c.591C=	ENSP00000352471.2:p.Arg197=
ENST00000375320.5:c.591C=	ENSP00000364469.1:p.Arg197=
ENST00000375323.5:c.591C=	ENSP00000364472.1:p.Arg197=
ENST00000375329.6:c.525C=	ENSP00000364478.2:p.Arg175=
NM_000039.1:c.591C= , LRG_767t1:c.591C=	NP_000030.1:p.Arg197=
XM_005271539.2:c.591C=	XP_005271596.1:p.Arg197=
XM_005271540.1:c.591C=	XP_005271597.1:p.Arg197=
NM_000039.2:c.591C=	NP_000030.1:p.Arg197=
NM_001318017.1:c.591C=	NP_001304946.1:p.Arg197=
NM_001318018.1:c.591C=	NP_001304947.1:p.Arg197=
NM_001318021.1:c.264C=	NP_001304950.1:p.Arg88=
NM_001318017.2:c.591C=	NP_001304946.1:p.Arg197=
NM_001318018.2:c.591C=	NP_001304947.1:p.Arg197=
NM_000039.3:c.591C= MANE Select	NP_000030.1:p.Arg197=