Canonical Allele Identifier: CA229325991
Gene: APOA1 HGNC NCBI
APOA1-AS HGNC NCBI

Linked Data

dbSNP Id: rs1799837

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116837537C>T , CM000673.2:g.116837537C>T GRCh38
NC_000011.9:g.116708253C>T , CM000673.1:g.116708253C>T GRCh37
NC_000011.8:g.116213463C>T NCBI36
NG_012021.1:g.5086G>A , LRG_767:g.5086G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000236850.5:c.-21+68G>A (APOA1) MANE Select ENSP00000236850.3:n.-21+68G>A
ENST00000236850.4:c.-21+68G>A (APOA1) ENSP00000236850.3:n.-21+68G>A
ENST00000359492.6:c.-21+22G>A (APOA1) ENSP00000352471.2:n.-21+22G>A
ENST00000375320.5:c.-30G>A (APOA1) ENSP00000364469.1:n.-30G>A
ENST00000375323.5:c.-150G>A (APOA1) ENSP00000364472.1:n.-150G>A
ENST00000375329.6:c.-59G>A (APOA1) ENSP00000364478.2:n.-59G>A
NM_000039.1:c.-21+68G>A , LRG_767t1:c.-21+68G>A (APOA1) NP_000030.1:n.-21+68G>A
NR_126362.1:n.123+1298C>T (APOA1-AS)
XM_005271539.2:c.-21+22G>A (APOA1) XP_005271596.1:n.-21+22G>A
XM_005271540.1:c.-30G>A (APOA1) XP_005271597.1:n.-30G>A
NM_000039.2:c.-21+68G>A (APOA1) NP_000030.1:n.-21+68G>A
NM_001318017.1:c.-30G>A (APOA1) NP_001304946.1:n.-30G>A
NM_001318018.1:c.-21+22G>A (APOA1) NP_001304947.1:n.-21+22G>A
NM_001318021.1:c.-304+68G>A (APOA1) NP_001304950.1:n.-304+68G>A
NM_001318017.2:c.-30G>A (APOA1) NP_001304946.1:n.-30G>A
NM_001318018.2:c.-21+22G>A (APOA1) NP_001304947.1:n.-21+22G>A
NM_000039.3:c.-21+68G>A (APOA1) MANE Select NP_000030.1:n.-21+68G>A