Canonical Allele Identifier: CA1619250635

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31657233_31657240delinsGGCTCTGT , CM000668.2:g.31657233_31657240delinsGGCTCTGT GRCh38
NC_000006.11:g.31625010_31625017delinsGGCTCTGT , CM000668.1:g.31625010_31625017delinsGGCTCTGT GRCh37
NC_000006.10:g.31732989_31732996delinsGGCTCTGT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375916.4:c.278_285delinsGGCTCTGT (APOM) MANE Select ENSP00000365081.3:p.Gly93=
ENST00000375916.3:c.278_285delinsGGCTCTGT ENSP00000365081.3:p.Gly93=
ENST00000375918.6:c.62_69delinsGGCTCTGT ENSP00000365083.2:p.Gly21=
ENST00000375920.8:c.62_69delinsGGCTCTGT ENSP00000365085.4:p.Gly21=
NM_001256169.1:c.62_69delinsGGCTCTGT (APOM) NP_001243098.1:p.Gly21=
NM_019101.2:c.278_285delinsGGCTCTGT (APOM) NP_061974.2:p.Gly93=
NR_045828.1:n.313_320delinsGGCTCTGT (APOM)
XM_006715150.2:c.182_189delinsGGCTCTGT (APOM) XP_006715213.1:p.Gly61=
XM_011514895.1:c.-14+3081_-14+3088delinsACAGAGCC (BAG6) XP_011513197.1:p.=
XM_006715150.3:c.182_189delinsGGCTCTGT (APOM) XP_006715213.1:p.Gly61=
XM_017011279.2:c.-14+3081_-14+3088delinsACAGAGCC (BAG6) XP_016866768.1:p.=
XM_024446545.1:c.-14+524_-14+531delinsACAGAGCC (BAG6) XP_024302313.1:p.=
NM_019101.3:c.278_285delinsGGCTCTGT (APOM) MANE Select NP_061974.2:p.Gly93=
NM_001256169.2:c.62_69delinsGGCTCTGT (APOM) NP_001243098.1:p.Gly21=
NR_045828.2:n.319_326delinsGGCTCTGT (APOM)