Canonical Allele Identifier: CA3478848
Gene: DIAPH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.141527722del , CM000667.2:g.141527722del GRCh38
NC_000005.9:g.140907289del , CM000667.1:g.140907289del GRCh37
NC_000005.8:g.140887473del NCBI36
NG_011594.1:g.96356del
NG_011594.2:g.96356del

Transcript Alleles

HGVS Amino-acid Change
ENST00000389054.8:c.3149-3del MANE Select ENSP00000373706.4:n.3149-3del
ENST00000647433.1:c.3149-3del ENSP00000494675.1:n.3149-3del
ENST00000253811.10:c.3017-3del ENSP00000253811.7:n.3017-3del
ENST00000389054.7:c.3149-3del ENSP00000373706.4:n.3149-3del
ENST00000389057.9:c.3122-3del ENSP00000373709.6:n.3122-3del
ENST00000398557.8:c.3149-3del ENSP00000381565.5:n.3149-3del
ENST00000518047.5:c.3122-3del ENSP00000428268.2:n.3122-3del
NM_001079812.2:c.3122-3del NP_001073280.1:n.3122-3del
NM_001314007.1:c.3149-3del NP_001300936.1:n.3149-3del
NM_005219.4:c.3149-3del NP_005210.3:n.3149-3del
XM_011537572.1:c.3113-3del XP_011535874.1:n.3113-3del
XM_011537573.1:c.3083-3del XP_011535875.1:n.3083-3del
XM_024454384.1:c.3149-3del XP_024310152.1:n.3149-3del
XM_024454385.1:c.3122-3del XP_024310153.1:n.3122-3del
XM_024454386.1:c.3113-3del XP_024310154.1:n.3113-3del
XM_024454387.1:c.3083-3del XP_024310155.1:n.3083-3del
NM_005219.5:c.3149-3del MANE Select NP_005210.3:n.3149-3del
NM_001079812.3:c.3122-3del NP_001073280.1:n.3122-3del
NM_001314007.2:c.3149-3del NP_001300936.1:n.3149-3del