Canonical Allele Identifier: CA402147842
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546409T>A , CM000680.2:g.31546409T>A GRCh38
NC_000018.9:g.29126372T>A , CM000680.1:g.29126372T>A GRCh37
NC_000018.8:g.27380370T>A NCBI36
NG_007072.3:g.53168T>A , LRG_397:g.53168T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261590.13:c.3023T>A (DSG2) MANE Select ENSP00000261590.8:p.Leu1008His
ENST00000261590.12:c.3023T>A (DSG2) ENSP00000261590.8:p.Leu1008His
NM_001943.3:c.3023T>A , LRG_397t1:c.3023T>A (DSG2) NP_001934.2:p.Leu1008His
NR_045216.1:n.1346-503A>T (DSG2-AS1)
NM_001943.4:c.3023T>A (DSG2) NP_001934.2:p.Leu1008His
XM_024451095.1:c.2489T>A (DSG2) XP_024306863.1:p.Leu830His
NM_001943.5:c.3023T>A (DSG2) MANE Select NP_001934.2:p.Leu1008His