Canonical Allele Identifier: CA2002761762
Gene: APOA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116835854_116835892delinsAAGCTGACCTTGAAGCTCTCCAGCACGGGCAGCAGGCCT , CM000673.2:g.116835854_116835892delinsAAGCTGACCTTGAAGCTCTCCAGCACGGGCAGCAGGCCT GRCh38
NC_000011.9:g.116706570_116706608delinsAAGCTGACCTTGAAGCTCTCCAGCACGGGCAGCAGGCCT , CM000673.1:g.116706570_116706608delinsAAGCTGACCTTGAAGCTCTCCAGCACGGGCAGCAGGCCT GRCh37
NC_000011.8:g.116211780_116211818delinsAAGCTGACCTTGAAGCTCTCCAGCACGGGCAGCAGGCCT NCBI36
NG_012021.1:g.6731_6769delinsAGGCCTGCTGCCCGTGCTGGAGAGCTTCAAGGTCAGCTT , LRG_767:g.6731_6769delinsAGGCCTGCTGCCCGTGCTGGAGAGCTTCAAGGTCAGCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000236850.5:c.720_758delinsAGGCCTGCTGCCCGTGCTGGAGAGCTTCAAGGTCAGCTT MANE Select ENSP00000236850.3:p.Gln240=
ENST00000236850.4:c.720_758delinsAGGCCTGCTGCCCGTGCTGGAGAGCTTCAAGGTCAGCTT ENSP00000236850.3:p.Gln240=
ENST00000359492.6:c.720_758delinsAGGCCTGCTGCCCGTGCTGGAGAGCTTCAAGGTCAGCTT ENSP00000352471.2:p.Gln240=
ENST00000375320.5:c.720_758delinsAGGCCTGCTGCCCGTGCTGGAGAGCTTCAAGGTCAGCTT ENSP00000364469.1:p.Gln240=
ENST00000375323.5:c.720_758delinsAGGCCTGCTGCCCGTGCTGGAGAGCTTCAAGGTCAGCTT ENSP00000364472.1:p.Gln240=
ENST00000375329.6:c.654_692delinsAGGCCTGCTGCCCGTGCTGGAGAGCTTCAAGGTCAGCTT ENSP00000364478.2:p.Gln218=
NM_000039.1:c.720_758delinsAGGCCTGCTGCCCGTGCTGGAGAGCTTCAAGGTCAGCTT , LRG_767t1:c.720_758delinsAGGCCTGCTGCCCGTGCTGGAGAGCTTCAAGGTCAGCTT NP_000030.1:p.Gln240=
XM_005271539.2:c.720_758delinsAGGCCTGCTGCCCGTGCTGGAGAGCTTCAAGGTCAGCTT XP_005271596.1:p.Gln240=
XM_005271540.1:c.720_758delinsAGGCCTGCTGCCCGTGCTGGAGAGCTTCAAGGTCAGCTT XP_005271597.1:p.Gln240=
NM_000039.2:c.720_758delinsAGGCCTGCTGCCCGTGCTGGAGAGCTTCAAGGTCAGCTT NP_000030.1:p.Gln240=
NM_001318017.1:c.720_758delinsAGGCCTGCTGCCCGTGCTGGAGAGCTTCAAGGTCAGCTT NP_001304946.1:p.Gln240=
NM_001318018.1:c.720_758delinsAGGCCTGCTGCCCGTGCTGGAGAGCTTCAAGGTCAGCTT NP_001304947.1:p.Gln240=
NM_001318021.1:c.393_431delinsAGGCCTGCTGCCCGTGCTGGAGAGCTTCAAGGTCAGCTT NP_001304950.1:p.Gln131=
NM_001318017.2:c.720_758delinsAGGCCTGCTGCCCGTGCTGGAGAGCTTCAAGGTCAGCTT NP_001304946.1:p.Gln240=
NM_001318018.2:c.720_758delinsAGGCCTGCTGCCCGTGCTGGAGAGCTTCAAGGTCAGCTT NP_001304947.1:p.Gln240=
NM_000039.3:c.720_758delinsAGGCCTGCTGCCCGTGCTGGAGAGCTTCAAGGTCAGCTT MANE Select NP_000030.1:p.Gln240=