Canonical Allele Identifier: CA2002761721

Gene: APOA1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116835787A= , CM000673.2:g.116835787A=	GRCh38
NC_000011.9:g.116706503A= , CM000673.1:g.116706503A=	GRCh37
NC_000011.8:g.116211713A=	NCBI36
NG_012021.1:g.6836T= , LRG_767:g.6836T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236850.5:c.*21T= MANE Select	ENSP00000236850.3:n.*21T=
ENST00000236850.4:c.*21T=	ENSP00000236850.3:n.*21T=
ENST00000359492.6:c.*21T=	ENSP00000352471.2:n.*21T=
ENST00000375320.5:c.*21T=	ENSP00000364469.1:n.*21T=
ENST00000375323.5:c.*21T=	ENSP00000364472.1:n.*21T=
ENST00000375329.6:c.*21T=	ENSP00000364478.2:n.*21T=
NM_000039.1:c.*21T= , LRG_767t1:c.*21T=	NP_000030.1:n.*21T=
XM_005271539.2:c.*21T=	XP_005271596.1:n.*21T=
XM_005271540.1:c.*21T=	XP_005271597.1:n.*21T=
NM_000039.2:c.*21T=	NP_000030.1:n.*21T=
NM_001318017.1:c.*21T=	NP_001304946.1:n.*21T=
NM_001318018.1:c.*21T=	NP_001304947.1:n.*21T=
NM_001318021.1:c.*21T=	NP_001304950.1:n.*21T=
NM_001318017.2:c.*21T=	NP_001304946.1:n.*21T=
NM_001318018.2:c.*21T=	NP_001304947.1:n.*21T=
NM_000039.3:c.*21T= MANE Select	NP_000030.1:n.*21T=