Canonical Allele Identifier: CA6289914

Gene: APOA1 APOA1-AS

Linked Data

• ClinVar Variation Id: 1935798
• ClinVar RCV Id: RCV002639094
• dbSNP Id: rs768618517
• ExAC: 11:116707891 G / A
• gnomAD v2: 11-116707891-G-A
• gnomAD v3: 11-116837175-G-A
• gnomAD v4: 11-116837175-G-A
• MyVariant Identifiers: chr11:g.116707891G>A (hg19) ; chr11:g.116837175G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116837175G>A , CM000673.2:g.116837175G>A	GRCh38
NC_000011.9:g.116707891G>A , CM000673.1:g.116707891G>A	GRCh37
NC_000011.8:g.116213101G>A	NCBI36
NG_012021.1:g.5448C>T , LRG_767:g.5448C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236850.5:c.44-18C>T (APOA1) MANE Select	ENSP00000236850.3:n.44-18C>T
ENST00000236850.4:c.44-18C>T (APOA1)	ENSP00000236850.3:n.44-18C>T
ENST00000359492.6:c.44-18C>T (APOA1)	ENSP00000352471.2:n.44-18C>T
ENST00000375320.5:c.44-18C>T (APOA1)	ENSP00000364469.1:n.44-18C>T
ENST00000375323.5:c.44-18C>T (APOA1)	ENSP00000364472.1:n.44-18C>T
ENST00000375329.6:c.134+170C>T (APOA1)	ENSP00000364478.2:n.134+170C>T
NM_000039.1:c.44-18C>T , LRG_767t1:c.44-18C>T (APOA1)	NP_000030.1:n.44-18C>T
NR_126362.1:n.123+936G>A (APOA1-AS)
XM_005271539.2:c.44-18C>T (APOA1)	XP_005271596.1:n.44-18C>T
XM_005271540.1:c.44-18C>T (APOA1)	XP_005271597.1:n.44-18C>T
NM_000039.2:c.44-18C>T (APOA1)	NP_000030.1:n.44-18C>T
NM_001318017.1:c.44-18C>T (APOA1)	NP_001304946.1:n.44-18C>T
NM_001318018.1:c.44-18C>T (APOA1)	NP_001304947.1:n.44-18C>T
NM_001318021.1:c.-240-62C>T (APOA1)	NP_001304950.1:n.-240-62C>T
NM_001318017.2:c.44-18C>T (APOA1)	NP_001304946.1:n.44-18C>T
NM_001318018.2:c.44-18C>T (APOA1)	NP_001304947.1:n.44-18C>T
NM_000039.3:c.44-18C>T (APOA1) MANE Select	NP_000030.1:n.44-18C>T