Canonical Allele Identifier: CA402127452
Gene: DSG1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.28906567A>T (hg19) chr18:g.31326604A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31326604A>T , CM000680.2:g.31326604A>T GRCh38
NC_000018.9:g.28906567A>T , CM000680.1:g.28906567A>T GRCh37
NC_000018.8:g.27160565A>T NCBI36
NG_011803.2:g.13516A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000257192.5:c.72A>T MANE Select ENSP00000257192.4:p.Glu24Asp
ENST00000257192.4:c.72A>T ENSP00000257192.4:p.Glu24Asp
NM_001942.3:c.72A>T NP_001933.2:p.Glu24Asp
NM_001942.4:c.72A>T MANE Select NP_001933.2:p.Glu24Asp
Search 100 bp 5'
Search 100 bp 3'