Canonical Allele Identifier: CA2002762501

Gene: APOA1 APOA1-AS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116837305_116837307delinsGCC , CM000673.2:g.116837305_116837307delinsGCC	GRCh38
NC_000011.9:g.116708021_116708023delinsGCC , CM000673.1:g.116708021_116708023delinsGCC	GRCh37
NC_000011.8:g.116213231_116213233delinsGCC	NCBI36
NG_012021.1:g.5316_5318delinsGGC , LRG_767:g.5316_5318delinsGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236850.5:c.43+38_43+40delinsGGC (APOA1) MANE Select	ENSP00000236850.3:n.43+38_43+40delinsGGC
ENST00000236850.4:c.43+38_43+40delinsGGC (APOA1)	ENSP00000236850.3:n.43+38_43+40delinsGGC
ENST00000359492.6:c.43+38_43+40delinsGGC (APOA1)	ENSP00000352471.2:n.43+38_43+40delinsGGC
ENST00000375320.5:c.43+38_43+40delinsGGC (APOA1)	ENSP00000364469.1:n.43+38_43+40delinsGGC
ENST00000375323.5:c.43+38_43+40delinsGGC (APOA1)	ENSP00000364472.1:n.43+38_43+40delinsGGC
ENST00000375329.6:c.134+38_134+40delinsGGC (APOA1)	ENSP00000364478.2:n.134+38_134+40delinsGGC
NM_000039.1:c.43+38_43+40delinsGGC , LRG_767t1:c.43+38_43+40delinsGGC (APOA1)	NP_000030.1:n.43+38_43+40delinsGGC
NR_126362.1:n.123+1066_123+1068delinsGCC (APOA1-AS)
XM_005271539.2:c.43+38_43+40delinsGGC (APOA1)	XP_005271596.1:n.43+38_43+40delinsGGC
XM_005271540.1:c.43+38_43+40delinsGGC (APOA1)	XP_005271597.1:n.43+38_43+40delinsGGC
NM_000039.2:c.43+38_43+40delinsGGC (APOA1)	NP_000030.1:n.43+38_43+40delinsGGC
NM_001318017.1:c.43+38_43+40delinsGGC (APOA1)	NP_001304946.1:n.43+38_43+40delinsGGC
NM_001318018.1:c.43+38_43+40delinsGGC (APOA1)	NP_001304947.1:n.43+38_43+40delinsGGC
NM_001318021.1:c.-241+38_-241+40delinsGGC (APOA1)	NP_001304950.1:n.-241+38_-241+40delinsGGC
NM_001318017.2:c.43+38_43+40delinsGGC (APOA1)	NP_001304946.1:n.43+38_43+40delinsGGC
NM_001318018.2:c.43+38_43+40delinsGGC (APOA1)	NP_001304947.1:n.43+38_43+40delinsGGC
NM_000039.3:c.43+38_43+40delinsGGC (APOA1) MANE Select	NP_000030.1:n.43+38_43+40delinsGGC