Canonical Allele Identifier: CA2677983702

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31657276del , CM000668.2:g.31657276del GRCh38
NC_000006.11:g.31625053del , CM000668.1:g.31625053del GRCh37
NC_000006.10:g.31733032del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000375916.4:c.321del (APOM) MANE Select ENSP00000365081.3:p.Ser108AlafsTer12
ENST00000375916.3:c.321del (APOM) ENSP00000365081.3:p.Ser108AlafsTer12
ENST00000375918.6:c.105del (APOM) ENSP00000365083.2:p.Ser36AlafsTer12
ENST00000375920.8:c.105del (APOM) ENSP00000365085.4:p.Ser36AlafsTer12
NM_001256169.1:c.105del (APOM) NP_001243098.1:p.Ser36AlafsTer12
NM_019101.2:c.321del (APOM) NP_061974.2:p.Ser108AlafsTer12
NR_045828.1:n.356del (APOM)
XM_006715150.2:c.225del (APOM) XP_006715213.1:p.Ser76AlafsTer12
XM_011514895.1:c.-14+3047del (BAG6) XP_011513197.1:n.-14+3047del
XM_006715150.3:c.225del (APOM) XP_006715213.1:p.Ser76AlafsTer12
XM_017011279.2:c.-14+3047del (BAG6) XP_016866768.1:n.-14+3047del
XM_024446545.1:c.-14+490del (BAG6) XP_024302313.1:n.-14+490del
NM_019101.3:c.321del (APOM) MANE Select NP_061974.2:p.Ser108AlafsTer12
NM_001256169.2:c.105del (APOM) NP_001243098.1:p.Ser36AlafsTer12
NR_045828.2:n.362del (APOM)