Canonical Allele Identifier: CA1085720338
Gene: DSP HGNC NCBI

Linked Data

dbSNP Id: rs61605193

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7554126_7554127insACACACACACACACACACACACA , CM000668.2:g.7554126_7554127insACACACACACACACACACACACA GRCh38
NC_000006.11:g.7554359_7554360insACACACACACACACACACACACA , CM000668.1:g.7554359_7554360insACACACACACACACACACACACA GRCh37
NC_000006.10:g.7499358_7499359insACACACACACACACACACACACA NCBI36
NG_008803.1:g.17490_17491insACACACACACACACACACACACA , LRG_423:g.17490_17491insACACACACACACACACACACACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000683682.2:c.171-1592_171-1591insACACACACACACACACACACACA ENSP00000508162.2:n.171-1592_171-1591insACACACACACACACACACACA...
ENST00000710359.1:c.171-1592_171-1591insACACACACACACACACACACACA ENSP00000518230.1:n.171-1592_171-1591insACACACACACACACACACACA...
ENST00000683563.1:n.63-1592_63-1591insACACACACACACACACACACACA
ENST00000683682.1:c.66-1592_66-1591insACACACACACACACACACACACA ENSP00000508162.1:n.66-1592_66-1591insACACACACACACACACACACACA...
ENST00000379802.8:c.171-1592_171-1591insACACACACACACACACACACACA MANE Select ENSP00000369129.3:n.171-1592_171-1591insACACACACACACACACACACA...
ENST00000379802.7:c.171-1592_171-1591insACACACACACACACACACACACA ENSP00000369129.3:n.171-1592_171-1591insACACACACACACACACACACA...
ENST00000418664.2:c.171-1592_171-1591insACACACACACACACACACACACA ENSP00000396591.2:n.171-1592_171-1591insACACACACACACACACACACA...
NM_001008844.1:c.171-1592_171-1591insACACACACACACACACACACACA NP_001008844.1:n.171-1592_171-1591insACACACACACACACACACACACA
NM_004415.2:c.171-1592_171-1591insACACACACACACACACACACACA , LRG_423t1:c.171-1592_171-1591insACACACACACACACACACACACA NP_004406.2:n.171-1592_171-1591insACACACACACACACACACACACA
XM_011514323.1:c.171-1592_171-1591insACACACACACACACACACACACA XP_011512625.1:n.171-1592_171-1591insACACACACACACACACACACACA
NM_001008844.2:c.171-1592_171-1591insACACACACACACACACACACACA NP_001008844.1:n.171-1592_171-1591insACACACACACACACACACACACA
NM_001319034.1:c.171-1592_171-1591insACACACACACACACACACACACA NP_001305963.1:n.171-1592_171-1591insACACACACACACACACACACACA
NM_004415.3:c.171-1592_171-1591insACACACACACACACACACACACA NP_004406.2:n.171-1592_171-1591insACACACACACACACACACACACA
NM_004415.4:c.171-1592_171-1591insACACACACACACACACACACACA MANE Select NP_004406.2:n.171-1592_171-1591insACACACACACACACACACACACA
NM_001008844.3:c.171-1592_171-1591insACACACACACACACACACACACA NP_001008844.1:n.171-1592_171-1591insACACACACACACACACACACACA
NM_001319034.2:c.171-1592_171-1591insACACACACACACACACACACACA NP_001305963.1:n.171-1592_171-1591insACACACACACACACACACACACA