Canonical Allele Identifier: CA382719376

Gene: APOA1 APOA1-AS

Linked Data

• MyVariant Identifiers: chr11:g.116707801G>T (hg19) ; chr11:g.116837085G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116837085G>T , CM000673.2:g.116837085G>T	GRCh38
NC_000011.9:g.116707801G>T , CM000673.1:g.116707801G>T	GRCh37
NC_000011.8:g.116213011G>T	NCBI36
NG_012021.1:g.5538C>A , LRG_767:g.5538C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236850.5:c.116C>A (APOA1) MANE Select	ENSP00000236850.3:p.Ala39Asp
ENST00000236850.4:c.116C>A (APOA1)	ENSP00000236850.3:p.Ala39Asp
ENST00000359492.6:c.116C>A (APOA1)	ENSP00000352471.2:p.Ala39Asp
ENST00000375320.5:c.116C>A (APOA1)	ENSP00000364469.1:p.Ala39Asp
ENST00000375323.5:c.116C>A (APOA1)	ENSP00000364472.1:p.Ala39Asp
ENST00000375329.6:c.134+260C>A (APOA1)	ENSP00000364478.2:n.134+260C>A
NM_000039.1:c.116C>A , LRG_767t1:c.116C>A (APOA1)	NP_000030.1:p.Ala39Asp
NR_126362.1:n.123+846G>T (APOA1-AS)
XM_005271539.2:c.116C>A (APOA1)	XP_005271596.1:p.Ala39Asp
XM_005271540.1:c.116C>A (APOA1)	XP_005271597.1:p.Ala39Asp
NM_000039.2:c.116C>A (APOA1)	NP_000030.1:p.Ala39Asp
NM_001318017.1:c.116C>A (APOA1)	NP_001304946.1:p.Ala39Asp
NM_001318018.1:c.116C>A (APOA1)	NP_001304947.1:p.Ala39Asp
NM_001318021.1:c.-212C>A (APOA1)	NP_001304950.1:n.-212C>A
NM_001318017.2:c.116C>A (APOA1)	NP_001304946.1:p.Ala39Asp
NM_001318018.2:c.116C>A (APOA1)	NP_001304947.1:p.Ala39Asp
NM_000039.3:c.116C>A (APOA1) MANE Select	NP_000030.1:p.Ala39Asp