Canonical Allele Identifier: CA2739268639
Gene: DSG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31524750_31524751delinsTG , CM000680.2:g.31524750_31524751delinsTG GRCh38
NC_000018.9:g.29104713_29104714delinsTG , CM000680.1:g.29104713_29104714delinsTG GRCh37
NC_000018.8:g.27358711_27358712delinsTG NCBI36
NG_007072.3:g.31509_31510delinsTG , LRG_397:g.31509_31510delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000682087.2:n.707_708delinsTG
ENST00000683614.2:n.707_708delinsTG
ENST00000682087.1:c.707_708delinsTG
ENST00000683614.1:c.707_708delinsTG
ENST00000261590.13:c.876_877delinsTG MANE Select ENSP00000261590.8:p.Ile293Val
ENST00000261590.12:c.876_877delinsTG ENSP00000261590.8:p.Ile293Val
NM_001943.3:c.876_877delinsTG , LRG_397t1:c.876_877delinsTG NP_001934.2:p.Ile293Val
NM_001943.4:c.876_877delinsTG NP_001934.2:p.Ile293Val
XM_024451095.1:c.342_343delinsTG XP_024306863.1:p.Ile115Val
NM_001943.5:c.876_877delinsTG MANE Select NP_001934.2:p.Ile293Val