Canonical Allele Identifier: CA2002762133
Gene: APOA1 HGNC NCBI
APOA1-AS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116836551C= , CM000673.2:g.116836551C= GRCh38
NC_000011.9:g.116707267C= , CM000673.1:g.116707267C= GRCh37
NC_000011.8:g.116212477C= NCBI36
NG_012021.1:g.6072G= , LRG_767:g.6072G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000236850.5:c.201-140G= (APOA1) MANE Select ENSP00000236850.3:n.201-140G=
ENST00000236850.4:c.201-140G= (APOA1) ENSP00000236850.3:n.201-140G=
ENST00000359492.6:c.201-140G= (APOA1) ENSP00000352471.2:n.201-140G=
ENST00000375320.5:c.201-140G= (APOA1) ENSP00000364469.1:n.201-140G=
ENST00000375323.5:c.201-140G= (APOA1) ENSP00000364472.1:n.201-140G=
ENST00000375329.6:c.135-140G= (APOA1) ENSP00000364478.2:n.135-140G=
NM_000039.1:c.201-140G= , LRG_767t1:c.201-140G= (APOA1) NP_000030.1:n.201-140G=
NR_126362.1:n.123+312C= (APOA1-AS)
XM_005271539.2:c.201-140G= (APOA1) XP_005271596.1:n.201-140G=
XM_005271540.1:c.201-140G= (APOA1) XP_005271597.1:n.201-140G=
NM_000039.2:c.201-140G= (APOA1) NP_000030.1:n.201-140G=
NM_001318017.1:c.201-140G= (APOA1) NP_001304946.1:n.201-140G=
NM_001318018.1:c.201-140G= (APOA1) NP_001304947.1:n.201-140G=
NM_001318021.1:c.-127-140G= (APOA1) NP_001304950.1:n.-127-140G=
NM_001318017.2:c.201-140G= (APOA1) NP_001304946.1:n.201-140G=
NM_001318018.2:c.201-140G= (APOA1) NP_001304947.1:n.201-140G=
NM_000039.3:c.201-140G= (APOA1) MANE Select NP_000030.1:n.201-140G=