Canonical Allele Identifier: CA2002761875

Gene: APOA1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116836064_116836074delinsAGCGCGTCCAC , CM000673.2:g.116836064_116836074delinsAGCGCGTCCAC	GRCh38
NC_000011.9:g.116706780_116706790delinsAGCGCGTCCAC , CM000673.1:g.116706780_116706790delinsAGCGCGTCCAC	GRCh37
NC_000011.8:g.116211990_116212000delinsAGCGCGTCCAC	NCBI36
NG_012021.1:g.6549_6559delinsGTGGACGCGCT , LRG_767:g.6549_6559delinsGTGGACGCGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236850.5:c.538_548delinsGTGGACGCGCT MANE Select	ENSP00000236850.3:p.Val180=
ENST00000236850.4:c.538_548delinsGTGGACGCGCT	ENSP00000236850.3:p.Val180=
ENST00000359492.6:c.538_548delinsGTGGACGCGCT	ENSP00000352471.2:p.Val180=
ENST00000375320.5:c.538_548delinsGTGGACGCGCT	ENSP00000364469.1:p.Val180=
ENST00000375323.5:c.538_548delinsGTGGACGCGCT	ENSP00000364472.1:p.Val180=
ENST00000375329.6:c.472_482delinsGTGGACGCGCT	ENSP00000364478.2:p.Val158=
NM_000039.1:c.538_548delinsGTGGACGCGCT , LRG_767t1:c.538_548delinsGTGGACGCGCT	NP_000030.1:p.Val180=
XM_005271539.2:c.538_548delinsGTGGACGCGCT	XP_005271596.1:p.Val180=
XM_005271540.1:c.538_548delinsGTGGACGCGCT	XP_005271597.1:p.Val180=
NM_000039.2:c.538_548delinsGTGGACGCGCT	NP_000030.1:p.Val180=
NM_001318017.1:c.538_548delinsGTGGACGCGCT	NP_001304946.1:p.Val180=
NM_001318018.1:c.538_548delinsGTGGACGCGCT	NP_001304947.1:p.Val180=
NM_001318021.1:c.211_221delinsGTGGACGCGCT	NP_001304950.1:p.Val71=
NM_001318017.2:c.538_548delinsGTGGACGCGCT	NP_001304946.1:p.Val180=
NM_001318018.2:c.538_548delinsGTGGACGCGCT	NP_001304947.1:p.Val180=
NM_000039.3:c.538_548delinsGTGGACGCGCT MANE Select	NP_000030.1:p.Val180=