Canonical Allele Identifier: CA2677983416

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31657130_31657131del , CM000668.2:g.31657130_31657131del GRCh38
NC_000006.11:g.31624907_31624908del , CM000668.1:g.31624907_31624908del GRCh37
NC_000006.10:g.31732886_31732887del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375916.4:c.270-95_270-94del (APOM) MANE Select ENSP00000365081.3:n.270-95_270-94del
ENST00000375916.3:c.270-95_270-94del (APOM) ENSP00000365081.3:n.270-95_270-94del
ENST00000375918.6:c.54-95_54-94del (APOM) ENSP00000365083.2:n.54-95_54-94del
ENST00000375920.8:c.54-95_54-94del (APOM) ENSP00000365085.4:n.54-95_54-94del
NM_001256169.1:c.54-95_54-94del (APOM) NP_001243098.1:n.54-95_54-94del
NM_019101.2:c.270-95_270-94del (APOM) NP_061974.2:n.270-95_270-94del
NR_045828.1:n.305-95_305-94del (APOM)
XM_006715150.2:c.174-95_174-94del (APOM) XP_006715213.1:n.174-95_174-94del
XM_011514895.1:c.-14+3192_-14+3193del (BAG6) XP_011513197.1:n.-14+3192_-14+3193del
XM_006715150.3:c.174-95_174-94del (APOM) XP_006715213.1:n.174-95_174-94del
XM_017011279.2:c.-14+3192_-14+3193del (BAG6) XP_016866768.1:n.-14+3192_-14+3193del
XM_024446545.1:c.-14+635_-14+636del (BAG6) XP_024302313.1:n.-14+635_-14+636del
NM_019101.3:c.270-95_270-94del (APOM) MANE Select NP_061974.2:n.270-95_270-94del
NM_001256169.2:c.54-95_54-94del (APOM) NP_001243098.1:n.54-95_54-94del
NR_045828.2:n.311-95_311-94del (APOM)