Canonical Allele Identifier: CA1619249686

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31654876_31654887delinsTTTAATCCTATA , CM000668.2:g.31654876_31654887delinsTTTAATCCTATA GRCh38
NC_000006.11:g.31622653_31622664delinsTTTAATCCTATA , CM000668.1:g.31622653_31622664delinsTTTAATCCTATA GRCh37
NC_000006.10:g.31730632_31730643delinsTTTAATCCTATA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375918.6:c.-102-1596_-102-1585delinsTTTAATCCTATA (APOM) ENSP00000365083.2:n.-102-1596_-102-1585de...
ENST00000375920.8:c.-102-1596_-102-1585delinsTTTAATCCTATA (APOM) ENSP00000365085.4:n.-102-1596_-102-1585de...
NM_001256169.1:c.-102-1596_-102-1585delinsTTTAATCCTATA (APOM) NP_001243098.1:n.-102-1596_-102-1585delin...
NR_045828.1:n.143-1596_143-1585delinsTTTAATCCTATA (APOM)
XM_011514895.1:c.-13-3111_-13-3100delinsTATAGGATTAAA (BAG6) XP_011513197.1:n.-13-3111_-13-3100delinsT...
XM_017011279.2:c.-13-3111_-13-3100delinsTATAGGATTAAA (BAG6) XP_016866768.1:n.-13-3111_-13-3100delinsT...
XM_024446545.1:c.-14+2877_-14+2888delinsTATAGGATTAAA (BAG6) XP_024302313.1:n.-14+2877_-14+2888delinsT...
NM_001256169.2:c.-102-1596_-102-1585delinsTTTAATCCTATA (APOM) NP_001243098.1:n.-102-1596_-102-1585delin...
NR_045828.2:n.149-1596_149-1585delinsTTTAATCCTATA (APOM)