Canonical Allele Identifier: CA2641407931
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31547247dup , CM000680.2:g.31547247dup GRCh38
NC_000018.9:g.29127210dup , CM000680.1:g.29127210dup GRCh37
NC_000018.8:g.27381208dup NCBI36
NG_007072.3:g.54006dup , LRG_397:g.54006dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.*504dup (DSG2) MANE Select ENSP00000261590.8:n.*504dup
ENST00000261590.12:c.*504dup (DSG2) ENSP00000261590.8:n.*504dup
NM_001943.3:c.*504dup , LRG_397t1:c.*504dup (DSG2) NP_001934.2:n.*504dup
NR_045216.1:n.1346-1340dup (DSG2-AS1)
NM_001943.4:c.*504dup (DSG2) NP_001934.2:n.*504dup
XM_024451095.1:c.*504dup (DSG2) XP_024306863.1:n.*504dup
NM_001943.5:c.*504dup (DSG2) MANE Select NP_001934.2:n.*504dup