Canonical Allele Identifier: CA1619250508

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31656982_31656983delinsTA , CM000668.2:g.31656982_31656983delinsTA GRCh38
NC_000006.11:g.31624759_31624760delinsTA , CM000668.1:g.31624759_31624760delinsTA GRCh37
NC_000006.10:g.31732738_31732739delinsTA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000375916.4:c.270-243_270-242delinsTA (APOM) MANE Select ENSP00000365081.3:n.270-243_270-242delinsTA
ENST00000375916.3:c.270-243_270-242delinsTA (APOM) ENSP00000365081.3:n.270-243_270-242delinsTA
ENST00000375918.6:c.54-243_54-242delinsTA (APOM) ENSP00000365083.2:n.54-243_54-242delinsTA
ENST00000375920.8:c.54-243_54-242delinsTA (APOM) ENSP00000365085.4:n.54-243_54-242delinsTA
NM_001256169.1:c.54-243_54-242delinsTA (APOM) NP_001243098.1:n.54-243_54-242delinsTA
NM_019101.2:c.270-243_270-242delinsTA (APOM) NP_061974.2:n.270-243_270-242delinsTA
NR_045828.1:n.305-243_305-242delinsTA (APOM)
XM_006715150.2:c.174-243_174-242delinsTA (APOM) XP_006715213.1:n.174-243_174-242delinsTA
XM_011514895.1:c.-14+3338_-14+3339delinsTA (BAG6) XP_011513197.1:n.-14+3338_-14+3339delinsTA
XM_006715150.3:c.174-243_174-242delinsTA (APOM) XP_006715213.1:n.174-243_174-242delinsTA
XM_017011279.2:c.-14+3338_-14+3339delinsTA (BAG6) XP_016866768.1:n.-14+3338_-14+3339delinsTA
XM_024446545.1:c.-14+781_-14+782delinsTA (BAG6) XP_024302313.1:n.-14+781_-14+782delinsTA
NM_019101.3:c.270-243_270-242delinsTA (APOM) MANE Select NP_061974.2:n.270-243_270-242delinsTA
NM_001256169.2:c.54-243_54-242delinsTA (APOM) NP_001243098.1:n.54-243_54-242delinsTA
NR_045828.2:n.311-243_311-242delinsTA (APOM)