Canonical Allele Identifier: CA2695215580

Gene: APOA1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116836020_116836052del , CM000673.2:g.116836020_116836052del	GRCh38
NC_000011.9:g.116706736_116706768del , CM000673.1:g.116706736_116706768del	GRCh37
NC_000011.8:g.116211946_116211978del	NCBI36
NG_012021.1:g.6576_6608del , LRG_767:g.6576_6608del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236850.5:c.565_597del MANE Select	ENSP00000236850.3:p.Pro189_Ala199del
ENST00000236850.4:c.565_597del	ENSP00000236850.3:p.Pro189_Ala199del
ENST00000359492.6:c.565_597del	ENSP00000352471.2:p.Pro189_Ala199del
ENST00000375320.5:c.565_597del	ENSP00000364469.1:p.Pro189_Ala199del
ENST00000375323.5:c.565_597del	ENSP00000364472.1:p.Pro189_Ala199del
ENST00000375329.6:c.499_531del	ENSP00000364478.2:p.Pro167_Ala177del
NM_000039.1:c.565_597del , LRG_767t1:c.565_597del	NP_000030.1:p.Pro189_Ala199del
XM_005271539.2:c.565_597del	XP_005271596.1:p.Pro189_Ala199del
XM_005271540.1:c.565_597del	XP_005271597.1:p.Pro189_Ala199del
NM_000039.2:c.565_597del	NP_000030.1:p.Pro189_Ala199del
NM_001318017.1:c.565_597del	NP_001304946.1:p.Pro189_Ala199del
NM_001318018.1:c.565_597del	NP_001304947.1:p.Pro189_Ala199del
NM_001318021.1:c.238_270del	NP_001304950.1:p.Pro80_Ala90del
NM_001318017.2:c.565_597del	NP_001304946.1:p.Pro189_Ala199del
NM_001318018.2:c.565_597del	NP_001304947.1:p.Pro189_Ala199del
NM_000039.3:c.565_597del MANE Select	NP_000030.1:p.Pro189_Ala199del