Canonical Allele Identifier: CA1619250572

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31657125_31657127delinsAAC , CM000668.2:g.31657125_31657127delinsAAC GRCh38
NC_000006.11:g.31624902_31624904delinsAAC , CM000668.1:g.31624902_31624904delinsAAC GRCh37
NC_000006.10:g.31732881_31732883delinsAAC NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375916.4:c.270-100_270-98delinsAAC (APOM) MANE Select ENSP00000365081.3:n.270-100_270-98delinsA...
ENST00000375916.3:c.270-100_270-98delinsAAC (APOM) ENSP00000365081.3:n.270-100_270-98delinsA...
ENST00000375918.6:c.54-100_54-98delinsAAC (APOM) ENSP00000365083.2:n.54-100_54-98delinsAAC...
ENST00000375920.8:c.54-100_54-98delinsAAC (APOM) ENSP00000365085.4:n.54-100_54-98delinsAAC...
NM_001256169.1:c.54-100_54-98delinsAAC (APOM) NP_001243098.1:n.54-100_54-98delinsAAC
NM_019101.2:c.270-100_270-98delinsAAC (APOM) NP_061974.2:n.270-100_270-98delinsAAC
NR_045828.1:n.305-100_305-98delinsAAC (APOM)
XM_006715150.2:c.174-100_174-98delinsAAC (APOM) XP_006715213.1:n.174-100_174-98delinsAAC
XM_011514895.1:c.-14+3194_-14+3196delinsGTT (BAG6) XP_011513197.1:n.-14+3194_-14+3196delinsG...
XM_006715150.3:c.174-100_174-98delinsAAC (APOM) XP_006715213.1:n.174-100_174-98delinsAAC
XM_017011279.2:c.-14+3194_-14+3196delinsGTT (BAG6) XP_016866768.1:n.-14+3194_-14+3196delinsG...
XM_024446545.1:c.-14+637_-14+639delinsGTT (BAG6) XP_024302313.1:n.-14+637_-14+639delinsGTT...
NM_019101.3:c.270-100_270-98delinsAAC (APOM) MANE Select NP_061974.2:n.270-100_270-98delinsAAC
NM_001256169.2:c.54-100_54-98delinsAAC (APOM) NP_001243098.1:n.54-100_54-98delinsAAC
NR_045828.2:n.311-100_311-98delinsAAC (APOM)