Canonical Allele Identifier: CA645580555
Gene: APOA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116836107_116836108delinsTT , CM000673.2:g.116836107_116836108delinsTT GRCh38
NC_000011.9:g.116706823_116706824delinsTT , CM000673.1:g.116706823_116706824delinsTT GRCh37
NC_000011.8:g.116212033_116212034delinsTT NCBI36
NG_012021.1:g.6515_6516delinsAA , LRG_767:g.6515_6516delinsAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000236850.5:c.504_505delinsAA MANE Select ENSP00000236850.3:p.Gly169Ser
ENST00000236850.4:c.504_505delinsAA ENSP00000236850.3:p.Gly169Ser
ENST00000359492.6:c.504_505delinsAA ENSP00000352471.2:p.Gly169Ser
ENST00000375320.5:c.504_505delinsAA ENSP00000364469.1:p.Gly169Ser
ENST00000375323.5:c.504_505delinsAA ENSP00000364472.1:p.Gly169Ser
ENST00000375329.6:c.438_439delinsAA ENSP00000364478.2:p.Gly147Ser
NM_000039.1:c.504_505delinsAA , LRG_767t1:c.504_505delinsAA NP_000030.1:p.Gly169Ser
XM_005271539.2:c.504_505delinsAA XP_005271596.1:p.Gly169Ser
XM_005271540.1:c.504_505delinsAA XP_005271597.1:p.Gly169Ser
NM_000039.2:c.504_505delinsAA NP_000030.1:p.Gly169Ser
NM_001318017.1:c.504_505delinsAA NP_001304946.1:p.Gly169Ser
NM_001318018.1:c.504_505delinsAA NP_001304947.1:p.Gly169Ser
NM_001318021.1:c.177_178delinsAA NP_001304950.1:p.Gly60Ser
NM_001318017.2:c.504_505delinsAA NP_001304946.1:p.Gly169Ser
NM_001318018.2:c.504_505delinsAA NP_001304947.1:p.Gly169Ser
NM_000039.3:c.504_505delinsAA MANE Select NP_000030.1:p.Gly169Ser