Canonical Allele Identifier: CA6289903
Gene: APOA1 HGNC NCBI
APOA1-AS HGNC NCBI

Linked Data

ClinVar Variation Id: 3127887
ClinVar RCV Id: RCV004417720
dbSNP Id: rs200213347

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116837122G>A , CM000673.2:g.116837122G>A GRCh38
NC_000011.9:g.116707838G>A , CM000673.1:g.116707838G>A GRCh37
NC_000011.8:g.116213048G>A NCBI36
NG_012021.1:g.5501C>T , LRG_767:g.5501C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000236850.5:c.79C>T (APOA1) MANE Select ENSP00000236850.3:p.Pro27Ser
ENST00000236850.4:c.79C>T (APOA1) ENSP00000236850.3:p.Pro27Ser
ENST00000359492.6:c.79C>T (APOA1) ENSP00000352471.2:p.Pro27Ser
ENST00000375320.5:c.79C>T (APOA1) ENSP00000364469.1:p.Pro27Ser
ENST00000375323.5:c.79C>T (APOA1) ENSP00000364472.1:p.Pro27Ser
ENST00000375329.6:c.134+223C>T (APOA1) ENSP00000364478.2:n.134+223C>T
NM_000039.1:c.79C>T , LRG_767t1:c.79C>T (APOA1) NP_000030.1:p.Pro27Ser
NR_126362.1:n.123+883G>A (APOA1-AS)
XM_005271539.2:c.79C>T (APOA1) XP_005271596.1:p.Pro27Ser
XM_005271540.1:c.79C>T (APOA1) XP_005271597.1:p.Pro27Ser
NM_000039.2:c.79C>T (APOA1) NP_000030.1:p.Pro27Ser
NM_001318017.1:c.79C>T (APOA1) NP_001304946.1:p.Pro27Ser
NM_001318018.1:c.79C>T (APOA1) NP_001304947.1:p.Pro27Ser
NM_001318021.1:c.-240-9C>T (APOA1) NP_001304950.1:n.-240-9C>T
NM_001318017.2:c.79C>T (APOA1) NP_001304946.1:p.Pro27Ser
NM_001318018.2:c.79C>T (APOA1) NP_001304947.1:p.Pro27Ser
NM_000039.3:c.79C>T (APOA1) MANE Select NP_000030.1:p.Pro27Ser