Canonical Allele Identifier: CA2611731015
Gene: DEAF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.686784_686787del , CM000673.2:g.686784_686787del GRCh38
NC_000011.9:g.686784_686787del , CM000673.1:g.686784_686787del GRCh37
NC_000011.8:g.676784_676787del NCBI36
NG_034156.1:g.13973_13976del
NG_034156.2:g.25302_25305del

Transcript Alleles

HGVS Amino-acid Change
ENST00000525626.6:n.689+76_689+79del
ENST00000528864.6:n.690+76_690+79del
ENST00000530813.2:c.*427+76_*427+79del ENSP00000508507.1:n.*427+76_*427+79del
ENST00000682936.1:n.564+76_564+79del
ENST00000683307.1:c.78+76_78+79del ENSP00000507198.1:n.78+76_78+79del
ENST00000684249.1:n.992+76_992+79del
ENST00000685854.1:c.600+76_600+79del ENSP00000508801.1:n.600+76_600+79del
ENST00000686001.1:c.600+76_600+79del ENSP00000508459.1:n.600+76_600+79del
ENST00000687329.1:c.600+76_600+79del ENSP00000510598.1:n.600+76_600+79del
ENST00000689835.1:c.600+76_600+79del ENSP00000510621.1:n.600+76_600+79del
ENST00000690068.1:c.600+76_600+79del ENSP00000509089.1:n.600+76_600+79del
ENST00000692634.1:c.600+76_600+79del ENSP00000508859.1:n.600+76_600+79del
ENST00000693164.1:n.798+76_798+79del
ENST00000382409.4:c.804+76_804+79del MANE Select ENSP00000371846.3:n.804+76_804+79del
ENST00000382409.3:c.804+76_804+79del ENSP00000371846.3:n.804+76_804+79del
ENST00000527170.5:c.166+76_166+79del
NM_001293634.1:c.664+1129_664+1132del NP_001280563.1:n.664+1129_664+1132del
NM_021008.3:c.804+76_804+79del NP_066288.2:n.804+76_804+79del
XM_011519842.1:c.804+76_804+79del XP_011518144.1:n.804+76_804+79del
XM_011519843.1:c.804+76_804+79del XP_011518145.1:n.804+76_804+79del
XR_428838.2:n.810+76_810+79del
XR_930843.1:n.810+76_810+79del
XM_011519842.3:c.804+76_804+79del XP_011518144.1:n.804+76_804+79del
XM_024448325.1:c.804+76_804+79del XP_024304093.1:n.804+76_804+79del
XM_024448326.1:c.804+76_804+79del XP_024304094.1:n.804+76_804+79del
XM_024448327.1:c.804+76_804+79del XP_024304095.1:n.804+76_804+79del
NM_001367390.1:c.78+76_78+79del NP_001354319.1:n.78+76_78+79del
NM_021008.4:c.804+76_804+79del MANE Select NP_066288.2:n.804+76_804+79del