Canonical Allele Identifier: CA2002761884

Gene: APOA1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116836078_116836080delinsGGC , CM000673.2:g.116836078_116836080delinsGGC	GRCh38
NC_000011.9:g.116706794_116706796delinsGGC , CM000673.1:g.116706794_116706796delinsGGC	GRCh37
NC_000011.8:g.116212004_116212006delinsGGC	NCBI36
NG_012021.1:g.6543_6545delinsGCC , LRG_767:g.6543_6545delinsGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236850.5:c.532_534delinsGCC MANE Select	ENSP00000236850.3:p.Ala178=
ENST00000236850.4:c.532_534delinsGCC	ENSP00000236850.3:p.Ala178=
ENST00000359492.6:c.532_534delinsGCC	ENSP00000352471.2:p.Ala178=
ENST00000375320.5:c.532_534delinsGCC	ENSP00000364469.1:p.Ala178=
ENST00000375323.5:c.532_534delinsGCC	ENSP00000364472.1:p.Ala178=
ENST00000375329.6:c.466_468delinsGCC	ENSP00000364478.2:p.Ala156=
NM_000039.1:c.532_534delinsGCC , LRG_767t1:c.532_534delinsGCC	NP_000030.1:p.Ala178=
XM_005271539.2:c.532_534delinsGCC	XP_005271596.1:p.Ala178=
XM_005271540.1:c.532_534delinsGCC	XP_005271597.1:p.Ala178=
NM_000039.2:c.532_534delinsGCC	NP_000030.1:p.Ala178=
NM_001318017.1:c.532_534delinsGCC	NP_001304946.1:p.Ala178=
NM_001318018.1:c.532_534delinsGCC	NP_001304947.1:p.Ala178=
NM_001318021.1:c.205_207delinsGCC	NP_001304950.1:p.Ala69=
NM_001318017.2:c.532_534delinsGCC	NP_001304946.1:p.Ala178=
NM_001318018.2:c.532_534delinsGCC	NP_001304947.1:p.Ala178=
NM_000039.3:c.532_534delinsGCC MANE Select	NP_000030.1:p.Ala178=