Canonical Allele Identifier: CA1087477224

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31657144_31657146del , CM000668.2:g.31657144_31657146del GRCh38
NC_000006.11:g.31624921_31624923del , CM000668.1:g.31624921_31624923del GRCh37
NC_000006.10:g.31732900_31732902del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375916.4:c.270-81_270-79del (APOM) MANE Select ENSP00000365081.3:n.270-81_270-79del
ENST00000375916.3:c.270-81_270-79del (APOM) ENSP00000365081.3:n.270-81_270-79del
ENST00000375918.6:c.54-81_54-79del (APOM) ENSP00000365083.2:n.54-81_54-79del
ENST00000375920.8:c.54-81_54-79del (APOM) ENSP00000365085.4:n.54-81_54-79del
NM_001256169.1:c.54-81_54-79del (APOM) NP_001243098.1:n.54-81_54-79del
NM_019101.2:c.270-81_270-79del (APOM) NP_061974.2:n.270-81_270-79del
NR_045828.1:n.305-81_305-79del (APOM)
XM_006715150.2:c.174-81_174-79del (APOM) XP_006715213.1:n.174-81_174-79del
XM_011514895.1:c.-14+3175_-14+3177del (BAG6) XP_011513197.1:n.-14+3175_-14+3177del
XM_006715150.3:c.174-81_174-79del (APOM) XP_006715213.1:n.174-81_174-79del
XM_017011279.2:c.-14+3175_-14+3177del (BAG6) XP_016866768.1:n.-14+3175_-14+3177del
XM_024446545.1:c.-14+618_-14+620del (BAG6) XP_024302313.1:n.-14+618_-14+620del
NM_019101.3:c.270-81_270-79del (APOM) MANE Select NP_061974.2:n.270-81_270-79del
NM_001256169.2:c.54-81_54-79del (APOM) NP_001243098.1:n.54-81_54-79del
NR_045828.2:n.311-81_311-79del (APOM)