Canonical Allele Identifier: CA2677982385

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31655832del , CM000668.2:g.31655832del GRCh38
NC_000006.11:g.31623609del , CM000668.1:g.31623609del GRCh37
NC_000006.10:g.31731588del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000375916.3:c.-135del (APOM) ENSP00000365081.3:n.-135del
ENST00000375918.6:c.-102-640del (APOM) ENSP00000365083.2:n.-102-640del
ENST00000375920.8:c.-102-640del (APOM) ENSP00000365085.4:n.-102-640del
NM_001256169.1:c.-102-640del (APOM) NP_001243098.1:n.-102-640del
NR_045828.1:n.143-640del (APOM)
XM_006715150.2:c.-238del (APOM) XP_006715213.1:n.-238del
XM_011514895.1:c.-13-4055del (BAG6) XP_011513197.1:n.-13-4055del
XM_017011279.2:c.-13-4055del (BAG6) XP_016866768.1:n.-13-4055del
XM_024446545.1:c.-14+1933del (BAG6) XP_024302313.1:n.-14+1933del
NM_001256169.2:c.-102-640del (APOM) NP_001243098.1:n.-102-640del
NR_045828.2:n.149-640del (APOM)