Canonical Allele Identifier: CA2002762321
Gene: APOA1 HGNC NCBI
APOA1-AS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116836961_116836962delinsGC , CM000673.2:g.116836961_116836962delinsGC GRCh38
NC_000011.9:g.116707677_116707678delinsGC , CM000673.1:g.116707677_116707678delinsGC GRCh37
NC_000011.8:g.116212887_116212888delinsGC NCBI36
NG_012021.1:g.5661_5662delinsGC , LRG_767:g.5661_5662delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000236850.5:c.200+39_200+40delinsGC (APOA1) MANE Select ENSP00000236850.3:n.200+39_200+40delinsGC
ENST00000236850.4:c.200+39_200+40delinsGC (APOA1) ENSP00000236850.3:n.200+39_200+40delinsGC
ENST00000359492.6:c.200+39_200+40delinsGC (APOA1) ENSP00000352471.2:n.200+39_200+40delinsGC
ENST00000375320.5:c.200+39_200+40delinsGC (APOA1) ENSP00000364469.1:n.200+39_200+40delinsGC
ENST00000375323.5:c.200+39_200+40delinsGC (APOA1) ENSP00000364472.1:n.200+39_200+40delinsGC
ENST00000375329.6:c.134+383_134+384delinsGC (APOA1) ENSP00000364478.2:n.134+383_134+384delinsGC
NM_000039.1:c.200+39_200+40delinsGC , LRG_767t1:c.200+39_200+40delinsGC (APOA1) NP_000030.1:n.200+39_200+40delinsGC
NR_126362.1:n.123+722_123+723delinsGC (APOA1-AS)
XM_005271539.2:c.200+39_200+40delinsGC (APOA1) XP_005271596.1:n.200+39_200+40delinsGC
XM_005271540.1:c.200+39_200+40delinsGC (APOA1) XP_005271597.1:n.200+39_200+40delinsGC
NM_000039.2:c.200+39_200+40delinsGC (APOA1) NP_000030.1:n.200+39_200+40delinsGC
NM_001318017.1:c.200+39_200+40delinsGC (APOA1) NP_001304946.1:n.200+39_200+40delinsGC
NM_001318018.1:c.200+39_200+40delinsGC (APOA1) NP_001304947.1:n.200+39_200+40delinsGC
NM_001318021.1:c.-128+39_-128+40delinsGC (APOA1) NP_001304950.1:n.-128+39_-128+40delinsGC
NM_001318017.2:c.200+39_200+40delinsGC (APOA1) NP_001304946.1:n.200+39_200+40delinsGC
NM_001318018.2:c.200+39_200+40delinsGC (APOA1) NP_001304947.1:n.200+39_200+40delinsGC
NM_000039.3:c.200+39_200+40delinsGC (APOA1) MANE Select NP_000030.1:n.200+39_200+40delinsGC