Canonical Allele Identifier: CA2002761829

Gene: APOA1

Linked Data

• dbSNP Id: rs1941532930

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116835988_116835990del , CM000673.2:g.116835988_116835990del	GRCh38
NC_000011.9:g.116706704_116706706del , CM000673.1:g.116706704_116706706del	GRCh37
NC_000011.8:g.116211914_116211916del	NCBI36
NG_012021.1:g.6633_6635del , LRG_767:g.6633_6635del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236850.5:c.622_624del MANE Select	ENSP00000236850.3:p.Asn208del
ENST00000236850.4:c.622_624del	ENSP00000236850.3:p.Asn208del
ENST00000359492.6:c.622_624del	ENSP00000352471.2:p.Asn208del
ENST00000375320.5:c.622_624del	ENSP00000364469.1:p.Asn208del
ENST00000375323.5:c.622_624del	ENSP00000364472.1:p.Asn208del
ENST00000375329.6:c.556_558del	ENSP00000364478.2:p.Asn186del
NM_000039.1:c.622_624del , LRG_767t1:c.622_624del	NP_000030.1:p.Asn208del
XM_005271539.2:c.622_624del	XP_005271596.1:p.Asn208del
XM_005271540.1:c.622_624del	XP_005271597.1:p.Asn208del
NM_000039.2:c.622_624del	NP_000030.1:p.Asn208del
NM_001318017.1:c.622_624del	NP_001304946.1:p.Asn208del
NM_001318018.1:c.622_624del	NP_001304947.1:p.Asn208del
NM_001318021.1:c.295_297del	NP_001304950.1:p.Asn99del
NM_001318017.2:c.622_624del	NP_001304946.1:p.Asn208del
NM_001318018.2:c.622_624del	NP_001304947.1:p.Asn208del
NM_000039.3:c.622_624del MANE Select	NP_000030.1:p.Asn208del