Canonical Allele Identifier: CA2293766632
Gene: DSG1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31326515T= , CM000680.2:g.31326515T= GRCh38
NC_000018.9:g.28906478T= , CM000680.1:g.28906478T= GRCh37
NC_000018.8:g.27160476T= NCBI36
NG_011803.2:g.13427T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000257192.5:c.49-66T= MANE Select ENSP00000257192.4:n.49-66T=
ENST00000257192.4:c.49-66T= ENSP00000257192.4:n.49-66T=
NM_001942.3:c.49-66T= NP_001933.2:n.49-66T=
NM_001942.4:c.49-66T= MANE Select NP_001933.2:n.49-66T=
Search 100 bp 5'
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