Canonical Allele Identifier: CA382715557

Gene: APOA1 APOA1-AS

Linked Data

• MyVariant Identifiers: chr11:g.116706841C>G (hg19) ; chr11:g.116836125C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116836125C>G , CM000673.2:g.116836125C>G	GRCh38
NC_000011.9:g.116706841C>G , CM000673.1:g.116706841C>G	GRCh37
NC_000011.8:g.116212051C>G	NCBI36
NG_012021.1:g.6498G>C , LRG_767:g.6498G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236850.5:c.487G>C (APOA1) MANE Select	ENSP00000236850.3:p.Glu163Gln
ENST00000236850.4:c.487G>C (APOA1)	ENSP00000236850.3:p.Glu163Gln
ENST00000359492.6:c.487G>C (APOA1)	ENSP00000352471.2:p.Glu163Gln
ENST00000375320.5:c.487G>C (APOA1)	ENSP00000364469.1:p.Glu163Gln
ENST00000375323.5:c.487G>C (APOA1)	ENSP00000364472.1:p.Glu163Gln
ENST00000375329.6:c.421G>C (APOA1)	ENSP00000364478.2:p.Glu141Gln
NM_000039.1:c.487G>C , LRG_767t1:c.487G>C (APOA1)	NP_000030.1:p.Glu163Gln
NR_126362.1:n.9C>G (APOA1-AS)
XM_005271539.2:c.487G>C (APOA1)	XP_005271596.1:p.Glu163Gln
XM_005271540.1:c.487G>C (APOA1)	XP_005271597.1:p.Glu163Gln
NM_000039.2:c.487G>C (APOA1)	NP_000030.1:p.Glu163Gln
NM_001318017.1:c.487G>C (APOA1)	NP_001304946.1:p.Glu163Gln
NM_001318018.1:c.487G>C (APOA1)	NP_001304947.1:p.Glu163Gln
NM_001318021.1:c.160G>C (APOA1)	NP_001304950.1:p.Glu54Gln
NM_001318017.2:c.487G>C (APOA1)	NP_001304946.1:p.Glu163Gln
NM_001318018.2:c.487G>C (APOA1)	NP_001304947.1:p.Glu163Gln
NM_000039.3:c.487G>C (APOA1) MANE Select	NP_000030.1:p.Glu163Gln