Canonical Allele Identifier: CA2616112004

Gene: APOA1

Linked Data

• gnomAD v4: 11-116836076-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116836079del , CM000673.2:g.116836079del	GRCh38
NC_000011.9:g.116706795del , CM000673.1:g.116706795del	GRCh37
NC_000011.8:g.116212005del	NCBI36
NG_012021.1:g.6546del , LRG_767:g.6546del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236850.5:c.535del MANE Select	ENSP00000236850.3:p.His179MetfsTer?
ENST00000236850.4:c.535del	ENSP00000236850.3:p.His179MetfsTer?
ENST00000359492.6:c.535del	ENSP00000352471.2:p.His179MetfsTer?
ENST00000375320.5:c.535del	ENSP00000364469.1:p.His179MetfsTer?
ENST00000375323.5:c.535del	ENSP00000364472.1:p.His179MetfsTer?
ENST00000375329.6:c.469del	ENSP00000364478.2:p.His157MetfsTer?
NM_000039.1:c.535del , LRG_767t1:c.535del	NP_000030.1:p.His179MetfsTer?
XM_005271539.2:c.535del	XP_005271596.1:p.His179MetfsTer?
XM_005271540.1:c.535del	XP_005271597.1:p.His179MetfsTer?
NM_000039.2:c.535del	NP_000030.1:p.His179MetfsTer?
NM_001318017.1:c.535del	NP_001304946.1:p.His179MetfsTer?
NM_001318018.1:c.535del	NP_001304947.1:p.His179MetfsTer?
NM_001318021.1:c.208del	NP_001304950.1:p.His70MetfsTer?
NM_001318017.2:c.535del	NP_001304946.1:p.His179MetfsTer?
NM_001318018.2:c.535del	NP_001304947.1:p.His179MetfsTer?
NM_000039.3:c.535del MANE Select	NP_000030.1:p.His179MetfsTer?