Canonical Allele Identifier: CA1608643482
Gene: DSP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7553866C= , CM000668.2:g.7553866C= GRCh38
NC_000006.11:g.7554099C= , CM000668.1:g.7554099C= GRCh37
NC_000006.10:g.7499098C= NCBI36
NG_008803.1:g.17230C= , LRG_423:g.17230C=

Transcript Alleles

HGVS Amino-acid change
ENST00000683682.2:c.171-1852C= ENSP00000508162.2:n.171-1852C=
ENST00000710359.1:c.171-1852C= ENSP00000518230.1:n.171-1852C=
ENST00000683563.1:n.63-1852C=
ENST00000683682.1:c.66-1852C= ENSP00000508162.1:n.66-1852C=
ENST00000379802.8:c.171-1852C= MANE Select ENSP00000369129.3:n.171-1852C=
ENST00000379802.7:c.171-1852C= ENSP00000369129.3:n.171-1852C=
ENST00000418664.2:c.171-1852C= ENSP00000396591.2:n.171-1852C=
NM_001008844.1:c.171-1852C= NP_001008844.1:n.171-1852C=
NM_004415.2:c.171-1852C= , LRG_423t1:c.171-1852C= NP_004406.2:n.171-1852C=
XM_011514323.1:c.171-1852C= XP_011512625.1:n.171-1852C=
NM_001008844.2:c.171-1852C= NP_001008844.1:n.171-1852C=
NM_001319034.1:c.171-1852C= NP_001305963.1:n.171-1852C=
NM_004415.3:c.171-1852C= NP_004406.2:n.171-1852C=
NM_004415.4:c.171-1852C= MANE Select NP_004406.2:n.171-1852C=
NM_001008844.3:c.171-1852C= NP_001008844.1:n.171-1852C=
NM_001319034.2:c.171-1852C= NP_001305963.1:n.171-1852C=