Canonical Allele Identifier: CA1608613634
Gene: DSP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7585199C= , CM000668.2:g.7585199C= GRCh38
NC_000006.11:g.7585432C= , CM000668.1:g.7585432C= GRCh37
NC_000006.10:g.7530431C= NCBI36
NG_008803.1:g.48563C= , LRG_423:g.48563C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000710359.1:c.6608C= ENSP00000518230.1:p.Thr2203=
ENST00000379802.8:c.7937C= MANE Select ENSP00000369129.3:p.Thr2646=
ENST00000379802.7:c.7937C= ENSP00000369129.3:p.Thr2646=
ENST00000418664.2:c.6140C= ENSP00000396591.2:p.Thr2047=
NM_001008844.1:c.6140C= NP_001008844.1:p.Thr2047=
NM_004415.2:c.7937C= , LRG_423t1:c.7937C= NP_004406.2:p.Thr2646=
XM_011514323.1:c.6608C= XP_011512625.1:p.Thr2203=
NM_001008844.2:c.6140C= NP_001008844.1:p.Thr2047=
NM_001319034.1:c.6608C= NP_001305963.1:p.Thr2203=
NM_004415.3:c.7937C= NP_004406.2:p.Thr2646=
NM_004415.4:c.7937C= MANE Select NP_004406.2:p.Thr2646=
NM_001008844.3:c.6140C= NP_001008844.1:p.Thr2047=
NM_001319034.2:c.6608C= NP_001305963.1:p.Thr2203=