Canonical Allele Identifier: CA2002761936

Gene: APOA1 APOA1-AS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116836163A= , CM000673.2:g.116836163A=	GRCh38
NC_000011.9:g.116706879A= , CM000673.1:g.116706879A=	GRCh37
NC_000011.8:g.116212089A=	NCBI36
NG_012021.1:g.6460T= , LRG_767:g.6460T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236850.5:c.449T= (APOA1) MANE Select	ENSP00000236850.3:p.Leu150=
ENST00000236850.4:c.449T= (APOA1)	ENSP00000236850.3:p.Leu150=
ENST00000359492.6:c.449T= (APOA1)	ENSP00000352471.2:p.Leu150=
ENST00000375320.5:c.449T= (APOA1)	ENSP00000364469.1:p.Leu150=
ENST00000375323.5:c.449T= (APOA1)	ENSP00000364472.1:p.Leu150=
ENST00000375329.6:c.383T= (APOA1)	ENSP00000364478.2:p.Leu128=
NM_000039.1:c.449T= , LRG_767t1:c.449T= (APOA1)	NP_000030.1:p.Leu150=
NR_126362.1:n.47A= (APOA1-AS)
XM_005271539.2:c.449T= (APOA1)	XP_005271596.1:p.Leu150=
XM_005271540.1:c.449T= (APOA1)	XP_005271597.1:p.Leu150=
NM_000039.2:c.449T= (APOA1)	NP_000030.1:p.Leu150=
NM_001318017.1:c.449T= (APOA1)	NP_001304946.1:p.Leu150=
NM_001318018.1:c.449T= (APOA1)	NP_001304947.1:p.Leu150=
NM_001318021.1:c.122T= (APOA1)	NP_001304950.1:p.Leu41=
NM_001318017.2:c.449T= (APOA1)	NP_001304946.1:p.Leu150=
NM_001318018.2:c.449T= (APOA1)	NP_001304947.1:p.Leu150=
NM_000039.3:c.449T= (APOA1) MANE Select	NP_000030.1:p.Leu150=