Canonical Allele Identifier: CA1085719644
Gene: DSP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7554099_7554126del , CM000668.2:g.7554099_7554126del GRCh38
NC_000006.11:g.7554332_7554359del , CM000668.1:g.7554332_7554359del GRCh37
NC_000006.10:g.7499331_7499358del NCBI36
NG_008803.1:g.17463_17490del , LRG_423:g.17463_17490del

Transcript Alleles

HGVS Amino-acid Change
ENST00000683682.2:c.171-1619_171-1592del ENSP00000508162.2:n.171-1619_171-1592del
ENST00000710359.1:c.171-1619_171-1592del ENSP00000518230.1:n.171-1619_171-1592del
ENST00000683563.1:n.63-1619_63-1592del
ENST00000683682.1:c.66-1619_66-1592del ENSP00000508162.1:n.66-1619_66-1592del
ENST00000379802.8:c.171-1619_171-1592del MANE Select ENSP00000369129.3:n.171-1619_171-1592del
ENST00000379802.7:c.171-1619_171-1592del ENSP00000369129.3:n.171-1619_171-1592del
ENST00000418664.2:c.171-1619_171-1592del ENSP00000396591.2:n.171-1619_171-1592del
NM_001008844.1:c.171-1619_171-1592del NP_001008844.1:n.171-1619_171-1592del
NM_004415.2:c.171-1619_171-1592del , LRG_423t1:c.171-1619_171-1592del NP_004406.2:n.171-1619_171-1592del
XM_011514323.1:c.171-1619_171-1592del XP_011512625.1:n.171-1619_171-1592del
NM_001008844.2:c.171-1619_171-1592del NP_001008844.1:n.171-1619_171-1592del
NM_001319034.1:c.171-1619_171-1592del NP_001305963.1:n.171-1619_171-1592del
NM_004415.3:c.171-1619_171-1592del NP_004406.2:n.171-1619_171-1592del
NM_004415.4:c.171-1619_171-1592del MANE Select NP_004406.2:n.171-1619_171-1592del
NM_001008844.3:c.171-1619_171-1592del NP_001008844.1:n.171-1619_171-1592del
NM_001319034.2:c.171-1619_171-1592del NP_001305963.1:n.171-1619_171-1592del