Canonical Allele Identifier: CA2695215582

Gene: APOA1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116836062_116836106del , CM000673.2:g.116836062_116836106del	GRCh38
NC_000011.9:g.116706778_116706822del , CM000673.1:g.116706778_116706822del	GRCh37
NC_000011.8:g.116211988_116212032del	NCBI36
NG_012021.1:g.6519_6563del , LRG_767:g.6519_6563del

Transcript Alleles

HGVS	Amino-acid change
ENST00000236850.5:c.508_552del MANE Select	ENSP00000236850.3:p.Glu170_Arg184del
ENST00000236850.4:c.508_552del	ENSP00000236850.3:p.Glu170_Arg184del
ENST00000359492.6:c.508_552del	ENSP00000352471.2:p.Glu170_Arg184del
ENST00000375320.5:c.508_552del	ENSP00000364469.1:p.Glu170_Arg184del
ENST00000375323.5:c.508_552del	ENSP00000364472.1:p.Glu170_Arg184del
ENST00000375329.6:c.442_486del	ENSP00000364478.2:p.Glu148_Arg162del
NM_000039.1:c.508_552del , LRG_767t1:c.508_552del	NP_000030.1:p.Glu170_Arg184del
XM_005271539.2:c.508_552del	XP_005271596.1:p.Glu170_Arg184del
XM_005271540.1:c.508_552del	XP_005271597.1:p.Glu170_Arg184del
NM_000039.2:c.508_552del	NP_000030.1:p.Glu170_Arg184del
NM_001318017.1:c.508_552del	NP_001304946.1:p.Glu170_Arg184del
NM_001318018.1:c.508_552del	NP_001304947.1:p.Glu170_Arg184del
NM_001318021.1:c.181_225del	NP_001304950.1:p.Glu61_Arg75del
NM_001318017.2:c.508_552del	NP_001304946.1:p.Glu170_Arg184del
NM_001318018.2:c.508_552del	NP_001304947.1:p.Glu170_Arg184del
NM_000039.3:c.508_552del MANE Select	NP_000030.1:p.Glu170_Arg184del