Canonical Allele Identifier: CA229324001

Gene: APOA1

Linked Data

• dbSNP Id: rs1038782960
• gnomAD v3: 11-116835949-G-T
• gnomAD v4: 11-116835949-G-T
• MyVariant Identifiers: chr11:g.116706665G>T (hg19) ; chr11:g.116835949G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116835949G>T , CM000673.2:g.116835949G>T	GRCh38
NC_000011.9:g.116706665G>T , CM000673.1:g.116706665G>T	GRCh37
NC_000011.8:g.116211875G>T	NCBI36
NG_012021.1:g.6674C>A , LRG_767:g.6674C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236850.5:c.663C>A MANE Select	ENSP00000236850.3:p.Thr221=
ENST00000236850.4:c.663C>A	ENSP00000236850.3:p.Thr221=
ENST00000359492.6:c.663C>A	ENSP00000352471.2:p.Thr221=
ENST00000375320.5:c.663C>A	ENSP00000364469.1:p.Thr221=
ENST00000375323.5:c.663C>A	ENSP00000364472.1:p.Thr221=
ENST00000375329.6:c.597C>A	ENSP00000364478.2:p.Thr199=
NM_000039.1:c.663C>A , LRG_767t1:c.663C>A	NP_000030.1:p.Thr221=
XM_005271539.2:c.663C>A	XP_005271596.1:p.Thr221=
XM_005271540.1:c.663C>A	XP_005271597.1:p.Thr221=
NM_000039.2:c.663C>A	NP_000030.1:p.Thr221=
NM_001318017.1:c.663C>A	NP_001304946.1:p.Thr221=
NM_001318018.1:c.663C>A	NP_001304947.1:p.Thr221=
NM_001318021.1:c.336C>A	NP_001304950.1:p.Thr112=
NM_001318017.2:c.663C>A	NP_001304946.1:p.Thr221=
NM_001318018.2:c.663C>A	NP_001304947.1:p.Thr221=
NM_000039.3:c.663C>A MANE Select	NP_000030.1:p.Thr221=