Canonical Allele Identifier: CA15690857
Gene: APOA1 HGNC NCBI
APOA1-AS HGNC NCBI

Linked Data

ClinVar Variation Id: 1239868
ClinVar RCV Id: RCV001637832
dbSNP Id: rs5069
gnomAD v2: 11-116708254-G-A
gnomAD v3: 11-116837538-G-A
gnomAD v4: 11-116837538-G-A
MyVariant Identifiers: chr11:g.116708254G>A (hg19) chr11:g.116837538G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116837538G>A , CM000673.2:g.116837538G>A GRCh38
NC_000011.9:g.116708254G>A , CM000673.1:g.116708254G>A GRCh37
NC_000011.8:g.116213464G>A NCBI36
NG_012021.1:g.5085C>T , LRG_767:g.5085C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000236850.5:c.-21+67C>T (APOA1) MANE Select ENSP00000236850.3:n.-21+67C>T
ENST00000236850.4:c.-21+67C>T (APOA1) ENSP00000236850.3:n.-21+67C>T
ENST00000359492.6:c.-21+21C>T (APOA1) ENSP00000352471.2:n.-21+21C>T
ENST00000375320.5:c.-31C>T (APOA1) ENSP00000364469.1:n.-31C>T
ENST00000375323.5:c.-151C>T (APOA1) ENSP00000364472.1:n.-151C>T
ENST00000375329.6:c.-60C>T (APOA1) ENSP00000364478.2:n.-60C>T
NM_000039.1:c.-21+67C>T , LRG_767t1:c.-21+67C>T (APOA1) NP_000030.1:n.-21+67C>T
NR_126362.1:n.123+1299G>A (APOA1-AS)
XM_005271539.2:c.-21+21C>T (APOA1) XP_005271596.1:n.-21+21C>T
XM_005271540.1:c.-31C>T (APOA1) XP_005271597.1:n.-31C>T
NM_000039.2:c.-21+67C>T (APOA1) NP_000030.1:n.-21+67C>T
NM_001318017.1:c.-31C>T (APOA1) NP_001304946.1:n.-31C>T
NM_001318018.1:c.-21+21C>T (APOA1) NP_001304947.1:n.-21+21C>T
NM_001318021.1:c.-304+67C>T (APOA1) NP_001304950.1:n.-304+67C>T
NM_001318017.2:c.-31C>T (APOA1) NP_001304946.1:n.-31C>T
NM_001318018.2:c.-21+21C>T (APOA1) NP_001304947.1:n.-21+21C>T
NM_000039.3:c.-21+67C>T (APOA1) MANE Select NP_000030.1:n.-21+67C>T
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