Canonical Allele Identifier: CA1619250596

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31657157_31657160delinsAAAG , CM000668.2:g.31657157_31657160delinsAAAG GRCh38
NC_000006.11:g.31624934_31624937delinsAAAG , CM000668.1:g.31624934_31624937delinsAAAG GRCh37
NC_000006.10:g.31732913_31732916delinsAAAG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375916.4:c.270-68_270-65delinsAAAG (APOM) MANE Select ENSP00000365081.3:n.270-68_270-65delinsAA...
ENST00000375916.3:c.270-68_270-65delinsAAAG (APOM) ENSP00000365081.3:n.270-68_270-65delinsAA...
ENST00000375918.6:c.54-68_54-65delinsAAAG (APOM) ENSP00000365083.2:n.54-68_54-65delinsAAAG...
ENST00000375920.8:c.54-68_54-65delinsAAAG (APOM) ENSP00000365085.4:n.54-68_54-65delinsAAAG...
NM_001256169.1:c.54-68_54-65delinsAAAG (APOM) NP_001243098.1:n.54-68_54-65delinsAAAG
NM_019101.2:c.270-68_270-65delinsAAAG (APOM) NP_061974.2:n.270-68_270-65delinsAAAG
NR_045828.1:n.305-68_305-65delinsAAAG (APOM)
XM_006715150.2:c.174-68_174-65delinsAAAG (APOM) XP_006715213.1:n.174-68_174-65delinsAAAG
XM_011514895.1:c.-14+3161_-14+3164delinsCTTT (BAG6) XP_011513197.1:n.-14+3161_-14+3164delinsC...
XM_006715150.3:c.174-68_174-65delinsAAAG (APOM) XP_006715213.1:n.174-68_174-65delinsAAAG
XM_017011279.2:c.-14+3161_-14+3164delinsCTTT (BAG6) XP_016866768.1:n.-14+3161_-14+3164delinsC...
XM_024446545.1:c.-14+604_-14+607delinsCTTT (BAG6) XP_024302313.1:n.-14+604_-14+607delinsCTT...
NM_019101.3:c.270-68_270-65delinsAAAG (APOM) MANE Select NP_061974.2:n.270-68_270-65delinsAAAG
NM_001256169.2:c.54-68_54-65delinsAAAG (APOM) NP_001243098.1:n.54-68_54-65delinsAAAG
NR_045828.2:n.311-68_311-65delinsAAAG (APOM)