Canonical Allele Identifier: CA1608643659
Gene: DSP HGNC NCBI

Linked Data

dbSNP Id: rs1554105404

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7554128_7554129insCCCCC , CM000668.2:g.7554128_7554129insCCCCC GRCh38
NC_000006.11:g.7554361_7554362insCCCCC , CM000668.1:g.7554361_7554362insCCCCC GRCh37
NC_000006.10:g.7499360_7499361insCCCCC NCBI36
NG_008803.1:g.17492_17493insCCCCC , LRG_423:g.17492_17493insCCCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000683682.2:c.171-1590_171-1589insCCCCC ENSP00000508162.2:n.171-1590_171-1589insCCCCC
ENST00000710359.1:c.171-1590_171-1589insCCCCC ENSP00000518230.1:n.171-1590_171-1589insCCCCC
ENST00000683563.1:n.63-1590_63-1589insCCCCC
ENST00000683682.1:c.66-1590_66-1589insCCCCC ENSP00000508162.1:n.66-1590_66-1589insCCCCC
ENST00000379802.8:c.171-1590_171-1589insCCCCC MANE Select ENSP00000369129.3:n.171-1590_171-1589insCCCCC
ENST00000379802.7:c.171-1590_171-1589insCCCCC ENSP00000369129.3:n.171-1590_171-1589insCCCCC
ENST00000418664.2:c.171-1590_171-1589insCCCCC ENSP00000396591.2:n.171-1590_171-1589insCCCCC
NM_001008844.1:c.171-1590_171-1589insCCCCC NP_001008844.1:n.171-1590_171-1589insCCCCC
NM_004415.2:c.171-1590_171-1589insCCCCC , LRG_423t1:c.171-1590_171-1589insCCCCC NP_004406.2:n.171-1590_171-1589insCCCCC
XM_011514323.1:c.171-1590_171-1589insCCCCC XP_011512625.1:n.171-1590_171-1589insCCCCC
NM_001008844.2:c.171-1590_171-1589insCCCCC NP_001008844.1:n.171-1590_171-1589insCCCCC
NM_001319034.1:c.171-1590_171-1589insCCCCC NP_001305963.1:n.171-1590_171-1589insCCCCC
NM_004415.3:c.171-1590_171-1589insCCCCC NP_004406.2:n.171-1590_171-1589insCCCCC
NM_004415.4:c.171-1590_171-1589insCCCCC MANE Select NP_004406.2:n.171-1590_171-1589insCCCCC
NM_001008844.3:c.171-1590_171-1589insCCCCC NP_001008844.1:n.171-1590_171-1589insCCCCC
NM_001319034.2:c.171-1590_171-1589insCCCCC NP_001305963.1:n.171-1590_171-1589insCCCCC