Canonical Allele Identifier: CA1608617176
Gene: DSP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7565420C= , CM000668.2:g.7565420C= GRCh38
NC_000006.11:g.7565653C= , CM000668.1:g.7565653C= GRCh37
NC_000006.10:g.7510652C= NCBI36
NG_008803.1:g.28784C= , LRG_423:g.28784C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000710359.1:c.839C= ENSP00000518230.1:p.Ser280=
ENST00000682228.1:n.163C=
ENST00000379802.8:c.839C= MANE Select ENSP00000369129.3:p.Ser280=
ENST00000379802.7:c.839C= ENSP00000369129.3:p.Ser280=
ENST00000418664.2:c.839C= ENSP00000396591.2:p.Ser280=
ENST00000506617.1:n.357C=
NM_001008844.1:c.839C= NP_001008844.1:p.Ser280=
NM_004415.2:c.839C= , LRG_423t1:c.839C= NP_004406.2:p.Ser280=
XM_011514323.1:c.839C= XP_011512625.1:p.Ser280=
NM_001008844.2:c.839C= NP_001008844.1:p.Ser280=
NM_001319034.1:c.839C= NP_001305963.1:p.Ser280=
NM_004415.3:c.839C= NP_004406.2:p.Ser280=
NM_004415.4:c.839C= MANE Select NP_004406.2:p.Ser280=
NM_001008844.3:c.839C= NP_001008844.1:p.Ser280=
NM_001319034.2:c.839C= NP_001305963.1:p.Ser280=