Canonical Allele Identifier: CA382715059

Gene: APOA1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116836023G>T , CM000673.2:g.116836023G>T	GRCh38
NC_000011.9:g.116706739G>T , CM000673.1:g.116706739G>T	GRCh37
NC_000011.8:g.116211949G>T	NCBI36
NG_012021.1:g.6600C>A , LRG_767:g.6600C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000039.3:c.589C>A MANE Select	NP_000030.1:p.Arg197Ser
ENST00000236850.5:c.589C>A MANE Select	ENSP00000236850.3:p.Arg197Ser
NM_000039.1:c.589C>A , LRG_767t1:c.589C>A	NP_000030.1:p.Arg197Ser
NM_000039.2:c.589C>A	NP_000030.1:p.Arg197Ser
NM_001318017.1:c.589C>A	NP_001304946.1:p.Arg197Ser
NM_001318017.2:c.589C>A	NP_001304946.1:p.Arg197Ser
NM_001318018.1:c.589C>A	NP_001304947.1:p.Arg197Ser
NM_001318018.2:c.589C>A	NP_001304947.1:p.Arg197Ser
NM_001318021.1:c.262C>A	NP_001304950.1:p.Arg88Ser
ENST00000236850.4:c.589C>A	ENSP00000236850.3:p.Arg197Ser
ENST00000359492.6:c.589C>A	ENSP00000352471.2:p.Arg197Ser
ENST00000375320.5:c.589C>A	ENSP00000364469.1:p.Arg197Ser
ENST00000375323.5:c.589C>A	ENSP00000364472.1:p.Arg197Ser
ENST00000375329.6:c.523C>A	ENSP00000364478.2:p.Arg175Ser
XM_005271539.2:c.589C>A	XP_005271596.1:p.Arg197Ser
XM_005271540.1:c.589C>A	XP_005271597.1:p.Arg197Ser