Canonical Allele Identifier: CA1085719729
Gene: DSP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7554119_7554125del , CM000668.2:g.7554119_7554125del GRCh38
NC_000006.11:g.7554352_7554358del , CM000668.1:g.7554352_7554358del GRCh37
NC_000006.10:g.7499351_7499357del NCBI36
NG_008803.1:g.17483_17489del , LRG_423:g.17483_17489del

Transcript Alleles

HGVS Amino-acid Change
ENST00000683682.2:c.171-1599_171-1593del ENSP00000508162.2:n.171-1599_171-1593del
ENST00000710359.1:c.171-1599_171-1593del ENSP00000518230.1:n.171-1599_171-1593del
ENST00000683563.1:n.63-1599_63-1593del
ENST00000683682.1:c.66-1599_66-1593del ENSP00000508162.1:n.66-1599_66-1593del
ENST00000379802.8:c.171-1599_171-1593del MANE Select ENSP00000369129.3:n.171-1599_171-1593del
ENST00000379802.7:c.171-1599_171-1593del ENSP00000369129.3:n.171-1599_171-1593del
ENST00000418664.2:c.171-1599_171-1593del ENSP00000396591.2:n.171-1599_171-1593del
NM_001008844.1:c.171-1599_171-1593del NP_001008844.1:n.171-1599_171-1593del
NM_004415.2:c.171-1599_171-1593del , LRG_423t1:c.171-1599_171-1593del NP_004406.2:n.171-1599_171-1593del
XM_011514323.1:c.171-1599_171-1593del XP_011512625.1:n.171-1599_171-1593del
NM_001008844.2:c.171-1599_171-1593del NP_001008844.1:n.171-1599_171-1593del
NM_001319034.1:c.171-1599_171-1593del NP_001305963.1:n.171-1599_171-1593del
NM_004415.3:c.171-1599_171-1593del NP_004406.2:n.171-1599_171-1593del
NM_004415.4:c.171-1599_171-1593del MANE Select NP_004406.2:n.171-1599_171-1593del
NM_001008844.3:c.171-1599_171-1593del NP_001008844.1:n.171-1599_171-1593del
NM_001319034.2:c.171-1599_171-1593del NP_001305963.1:n.171-1599_171-1593del