Canonical Allele Identifier: CA2575000166

Gene: APOA1

Linked Data

• gnomAD v4: 11-116835757-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116835757C>T , CM000673.2:g.116835757C>T	GRCh38
NC_000011.9:g.116706473C>T , CM000673.1:g.116706473C>T	GRCh37
NC_000011.8:g.116211683C>T	NCBI36
NG_012021.1:g.6866G>A , LRG_767:g.6866G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236850.5:c.*51G>A MANE Select	ENSP00000236850.3:n.*51G>A
ENST00000236850.4:c.*51G>A	ENSP00000236850.3:n.*51G>A
ENST00000359492.6:c.*51G>A	ENSP00000352471.2:n.*51G>A
ENST00000375320.5:c.*51G>A	ENSP00000364469.1:n.*51G>A
ENST00000375323.5:c.*51G>A	ENSP00000364472.1:n.*51G>A
ENST00000375329.6:c.*51G>A	ENSP00000364478.2:n.*51G>A
NM_000039.1:c.*51G>A , LRG_767t1:c.*51G>A	NP_000030.1:n.*51G>A
XM_005271539.2:c.*51G>A	XP_005271596.1:n.*51G>A
XM_005271540.1:c.*51G>A	XP_005271597.1:n.*51G>A
NM_000039.2:c.*51G>A	NP_000030.1:n.*51G>A
NM_001318017.1:c.*51G>A	NP_001304946.1:n.*51G>A
NM_001318018.1:c.*51G>A	NP_001304947.1:n.*51G>A
NM_001318021.1:c.*51G>A	NP_001304950.1:n.*51G>A
NM_001318017.2:c.*51G>A	NP_001304946.1:n.*51G>A
NM_001318018.2:c.*51G>A	NP_001304947.1:n.*51G>A
NM_000039.3:c.*51G>A MANE Select	NP_000030.1:n.*51G>A