Canonical Allele Identifier: CA1608615615
Gene: DSP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7580028T= , CM000668.2:g.7580028T= GRCh38
NC_000006.11:g.7580261T= , CM000668.1:g.7580261T= GRCh37
NC_000006.10:g.7525260T= NCBI36
NG_008803.1:g.43392T= , LRG_423:g.43392T=

Transcript Alleles

HGVS Amino-acid change
ENST00000710359.1:c.3838T= ENSP00000518230.1:p.Cys1280=
ENST00000379802.8:c.3838T= MANE Select ENSP00000369129.3:p.Cys1280=
ENST00000379802.7:c.3838T= ENSP00000369129.3:p.Cys1280=
ENST00000418664.2:c.3582+256T= ENSP00000396591.2:n.3582+256T=
NM_001008844.1:c.3582+256T= NP_001008844.1:n.3582+256T=
NM_004415.2:c.3838T= , LRG_423t1:c.3838T= NP_004406.2:p.Cys1280=
XM_011514323.1:c.3838T= XP_011512625.1:p.Cys1280=
NM_001008844.2:c.3582+256T= NP_001008844.1:n.3582+256T=
NM_001319034.1:c.3838T= NP_001305963.1:p.Cys1280=
NM_004415.3:c.3838T= NP_004406.2:p.Cys1280=
NM_004415.4:c.3838T= MANE Select NP_004406.2:p.Cys1280=
NM_001008844.3:c.3582+256T= NP_001008844.1:n.3582+256T=
NM_001319034.2:c.3838T= NP_001305963.1:p.Cys1280=