Canonical Allele Identifier: CA2293766659
Gene: DSG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31326568T= , CM000680.2:g.31326568T= GRCh38
NC_000018.9:g.28906531T= , CM000680.1:g.28906531T= GRCh37
NC_000018.8:g.27160529T= NCBI36
NG_011803.2:g.13480T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000257192.5:c.49-13T= MANE Select ENSP00000257192.4:n.49-13T=
ENST00000257192.4:c.49-13T= ENSP00000257192.4:n.49-13T=
NM_001942.3:c.49-13T= NP_001933.2:n.49-13T=
NM_001942.4:c.49-13T= MANE Select NP_001933.2:n.49-13T=