Canonical Allele Identifier: CA2695205994
Gene: DSP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7565413del , CM000668.2:g.7565413del GRCh38
NC_000006.11:g.7565646del , CM000668.1:g.7565646del GRCh37
NC_000006.10:g.7510645del NCBI36
NG_008803.1:g.28777del , LRG_423:g.28777del

Transcript Alleles

HGVS Amino-acid Change
ENST00000710359.1:c.832del ENSP00000518230.1:p.Ala278ProfsTer?
ENST00000682228.1:n.156del
ENST00000379802.8:c.832del MANE Select ENSP00000369129.3:p.Ala278ProfsTer?
ENST00000379802.7:c.832del ENSP00000369129.3:p.Ala278ProfsTer?
ENST00000418664.2:c.832del ENSP00000396591.2:p.Ala278ProfsTer?
ENST00000506617.1:n.350del
NM_001008844.1:c.832del NP_001008844.1:p.Ala278ProfsTer?
NM_004415.2:c.832del , LRG_423t1:c.832del NP_004406.2:p.Ala278ProfsTer?
XM_011514323.1:c.832del XP_011512625.1:p.Ala278ProfsTer?
NM_001008844.2:c.832del NP_001008844.1:p.Ala278ProfsTer?
NM_001319034.1:c.832del NP_001305963.1:p.Ala278ProfsTer?
NM_004415.3:c.832del NP_004406.2:p.Ala278ProfsTer?
NM_004415.4:c.832del MANE Select NP_004406.2:p.Ala278ProfsTer?
NM_001008844.3:c.832del NP_001008844.1:p.Ala278ProfsTer?
NM_001319034.2:c.832del NP_001305963.1:p.Ala278ProfsTer?