Canonical Allele Identifier: CA1085719777
Gene: DSP HGNC NCBI

Linked Data

dbSNP Id: rs1364448993

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7554126_7554127insACACACACACACACACACACACACACCCAC , CM000668.2:g.7554126_7554127insACACACACACACACACACACACACACCCAC GRCh38
NC_000006.11:g.7554359_7554360insACACACACACACACACACACACACACCCAC , CM000668.1:g.7554359_7554360insACACACACACACACACACACACACACCCAC GRCh37
NC_000006.10:g.7499358_7499359insACACACACACACACACACACACACACCCAC NCBI36
NG_008803.1:g.17490_17491insACACACACACACACACACACACACACCCAC , LRG_423:g.17490_17491insACACACACACACACACACACACACACCCAC

Transcript Alleles

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