Canonical Allele Identifier: CA2002762313

Gene: APOA1 APOA1-AS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116836943A= , CM000673.2:g.116836943A=	GRCh38
NC_000011.9:g.116707659A= , CM000673.1:g.116707659A=	GRCh37
NC_000011.8:g.116212869A=	NCBI36
NG_012021.1:g.5680T= , LRG_767:g.5680T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236850.5:c.200+58T= (APOA1) MANE Select	ENSP00000236850.3:n.200+58T=
ENST00000236850.4:c.200+58T= (APOA1)	ENSP00000236850.3:n.200+58T=
ENST00000359492.6:c.200+58T= (APOA1)	ENSP00000352471.2:n.200+58T=
ENST00000375320.5:c.200+58T= (APOA1)	ENSP00000364469.1:n.200+58T=
ENST00000375323.5:c.200+58T= (APOA1)	ENSP00000364472.1:n.200+58T=
ENST00000375329.6:c.134+402T= (APOA1)	ENSP00000364478.2:n.134+402T=
NM_000039.1:c.200+58T= , LRG_767t1:c.200+58T= (APOA1)	NP_000030.1:n.200+58T=
NR_126362.1:n.123+704A= (APOA1-AS)
XM_005271539.2:c.200+58T= (APOA1)	XP_005271596.1:n.200+58T=
XM_005271540.1:c.200+58T= (APOA1)	XP_005271597.1:n.200+58T=
NM_000039.2:c.200+58T= (APOA1)	NP_000030.1:n.200+58T=
NM_001318017.1:c.200+58T= (APOA1)	NP_001304946.1:n.200+58T=
NM_001318018.1:c.200+58T= (APOA1)	NP_001304947.1:n.200+58T=
NM_001318021.1:c.-128+58T= (APOA1)	NP_001304950.1:n.-128+58T=
NM_001318017.2:c.200+58T= (APOA1)	NP_001304946.1:n.200+58T=
NM_001318018.2:c.200+58T= (APOA1)	NP_001304947.1:n.200+58T=
NM_000039.3:c.200+58T= (APOA1) MANE Select	NP_000030.1:n.200+58T=