Canonical Allele Identifier: CA1619250738

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31657475_31657477delinsTAC , CM000668.2:g.31657475_31657477delinsTAC GRCh38
NC_000006.11:g.31625252_31625254delinsTAC , CM000668.1:g.31625252_31625254delinsTAC GRCh37
NC_000006.10:g.31733231_31733233delinsTAC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000375916.4:c.439_441delinsTAC (APOM) MANE Select ENSP00000365081.3:p.Tyr147=
ENST00000375916.3:c.439_441delinsTAC (APOM) ENSP00000365081.3:p.Tyr147=
ENST00000375918.6:c.223_225delinsTAC (APOM) ENSP00000365083.2:p.Tyr75=
ENST00000375920.8:c.223_225delinsTAC (APOM) ENSP00000365085.4:p.Tyr75=
NM_001256169.1:c.223_225delinsTAC (APOM) NP_001243098.1:p.Tyr75=
NM_019101.2:c.439_441delinsTAC (APOM) NP_061974.2:p.Tyr147=
NR_045828.1:n.474_476delinsTAC (APOM)
XM_006715150.2:c.343_345delinsTAC (APOM) XP_006715213.1:p.Tyr115=
XM_011514895.1:c.-14+2844_-14+2846delinsGTA (BAG6) XP_011513197.1:n.-14+2844_-14+2846delinsGTA
XM_006715150.3:c.343_345delinsTAC (APOM) XP_006715213.1:p.Tyr115=
XM_017011279.2:c.-14+2844_-14+2846delinsGTA (BAG6) XP_016866768.1:n.-14+2844_-14+2846delinsGTA
XM_024446545.1:c.-14+287_-14+289delinsGTA (BAG6) XP_024302313.1:n.-14+287_-14+289delinsGTA
NM_019101.3:c.439_441delinsTAC (APOM) MANE Select NP_061974.2:p.Tyr147=
NM_001256169.2:c.223_225delinsTAC (APOM) NP_001243098.1:p.Tyr75=
NR_045828.2:n.480_482delinsTAC (APOM)