Canonical Allele Identifier: CA127577
Gene: APOA1 HGNC NCBI
APOA1-AS HGNC NCBI

Linked Data

ClinVar Variation Id: 17928
ClinVar RCV Id: RCV000019521
dbSNP Id: rs121912726

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116836392A>G , CM000673.2:g.116836392A>G GRCh38
NC_000011.9:g.116707108A>G , CM000673.1:g.116707108A>G GRCh37
NC_000011.8:g.116212318A>G NCBI36
NG_012021.1:g.6231T>C , LRG_767:g.6231T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000236850.5:c.220T>C (APOA1) MANE Select ENSP00000236850.3:p.Trp74Arg
ENST00000236850.4:c.220T>C (APOA1) ENSP00000236850.3:p.Trp74Arg
ENST00000359492.6:c.220T>C (APOA1) ENSP00000352471.2:p.Trp74Arg
ENST00000375320.5:c.220T>C (APOA1) ENSP00000364469.1:p.Trp74Arg
ENST00000375323.5:c.220T>C (APOA1) ENSP00000364472.1:p.Trp74Arg
ENST00000375329.6:c.154T>C (APOA1) ENSP00000364478.2:p.Trp52Arg
NM_000039.1:c.220T>C , LRG_767t1:c.220T>C (APOA1) NP_000030.1:p.Trp74Arg
NR_126362.1:n.123+153A>G (APOA1-AS)
XM_005271539.2:c.220T>C (APOA1) XP_005271596.1:p.Trp74Arg
XM_005271540.1:c.220T>C (APOA1) XP_005271597.1:p.Trp74Arg
NM_000039.2:c.220T>C (APOA1) NP_000030.1:p.Trp74Arg
NM_001318017.1:c.220T>C (APOA1) NP_001304946.1:p.Trp74Arg
NM_001318018.1:c.220T>C (APOA1) NP_001304947.1:p.Trp74Arg
NM_001318021.1:c.-108T>C (APOA1) NP_001304950.1:n.-108T>C
NM_001318017.2:c.220T>C (APOA1) NP_001304946.1:p.Trp74Arg
NM_001318018.2:c.220T>C (APOA1) NP_001304947.1:p.Trp74Arg
NM_000039.3:c.220T>C (APOA1) MANE Select NP_000030.1:p.Trp74Arg