Canonical Allele Identifier: CA565105476
Gene: DSP HGNC NCBI

Linked Data

dbSNP Id: rs1311913546
gnomAD v2: 6-7577289-ATAAAGAATGTTG-A
MyVariant Identifiers: chr6:g.7577290_7577301del (hg19) chr6:g.7577057_7577068del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7577057_7577068del , CM000668.2:g.7577057_7577068del GRCh38
NC_000006.11:g.7577290_7577301del , CM000668.1:g.7577290_7577301del GRCh37
NC_000006.10:g.7522289_7522300del NCBI36
NG_008803.1:g.40421_40432del , LRG_423:g.40421_40432del

Transcript Alleles

HGVS Amino-acid change
ENST00000710359.1:c.2877+15_2877+26del ENSP00000518230.1:n.2877+15_2877+26del
ENST00000379802.8:c.2877+15_2877+26del MANE Select ENSP00000369129.3:n.2877+15_2877+26del
ENST00000379802.7:c.2877+15_2877+26del ENSP00000369129.3:n.2877+15_2877+26del
ENST00000418664.2:c.2877+15_2877+26del ENSP00000396591.2:n.2877+15_2877+26del
NM_001008844.1:c.2877+15_2877+26del NP_001008844.1:n.2877+15_2877+26del
NM_004415.2:c.2877+15_2877+26del , LRG_423t1:c.2877+15_2877+26del NP_004406.2:n.2877+15_2877+26del
XM_011514323.1:c.2877+15_2877+26del XP_011512625.1:n.2877+15_2877+26del
NM_001008844.2:c.2877+15_2877+26del NP_001008844.1:n.2877+15_2877+26del
NM_001319034.1:c.2877+15_2877+26del NP_001305963.1:n.2877+15_2877+26del
NM_004415.3:c.2877+15_2877+26del NP_004406.2:n.2877+15_2877+26del
NM_004415.4:c.2877+15_2877+26del MANE Select NP_004406.2:n.2877+15_2877+26del
NM_001008844.3:c.2877+15_2877+26del NP_001008844.1:n.2877+15_2877+26del
NM_001319034.2:c.2877+15_2877+26del NP_001305963.1:n.2877+15_2877+26del
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