Canonical Allele Identifier: CA2675691749
Gene: DIAPH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.141573822_141573893del , CM000667.2:g.141573822_141573893del GRCh38
NC_000005.9:g.140953389_140953460del , CM000667.1:g.140953389_140953460del GRCh37
NC_000005.8:g.140933573_140933644del NCBI36
NG_011594.1:g.50168_50239del
NG_011594.2:g.50168_50239del

Transcript Alleles

HGVS Amino-acid Change
ENST00000389054.8:c.1962_2033del MANE Select ENSP00000373706.4:p.Pro655_Pro678del
ENST00000647433.1:c.1962_2033del ENSP00000494675.1:p.Pro655_Pro678del
ENST00000253811.10:c.1830_1901del ENSP00000253811.7:p.Pro611_Pro634del
ENST00000389054.7:c.1962_2033del ENSP00000373706.4:p.Pro655_Pro678del
ENST00000389057.9:c.1935_2006del ENSP00000373709.6:p.Pro646_Pro669del
ENST00000398557.8:c.1962_2033del ENSP00000381565.5:p.Pro655_Pro678del
ENST00000518047.5:c.1935_2006del ENSP00000428268.2:p.Pro646_Pro669del
NM_001079812.2:c.1935_2006del NP_001073280.1:p.Pro646_Pro669del
NM_001314007.1:c.1962_2033del NP_001300936.1:p.Pro655_Pro678del
NM_005219.4:c.1962_2033del NP_005210.3:p.Pro655_Pro678del
XM_011537572.1:c.1926_1997del XP_011535874.1:p.Pro643_Pro666del
XM_011537573.1:c.1896_1967del XP_011535875.1:p.Pro633_Pro656del
XM_024454384.1:c.1962_2033del XP_024310152.1:p.Pro655_Pro678del
XM_024454385.1:c.1935_2006del XP_024310153.1:p.Pro646_Pro669del
XM_024454386.1:c.1926_1997del XP_024310154.1:p.Pro643_Pro666del
XM_024454387.1:c.1896_1967del XP_024310155.1:p.Pro633_Pro656del
NM_005219.5:c.1962_2033del MANE Select NP_005210.3:p.Pro655_Pro678del
NM_001079812.3:c.1935_2006del NP_001073280.1:p.Pro646_Pro669del
NM_001314007.2:c.1962_2033del NP_001300936.1:p.Pro655_Pro678del