Canonical Allele Identifier: CA988914043
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs2073320015

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31547290_31547292dup , CM000680.2:g.31547290_31547292dup GRCh38
NC_000018.9:g.29127253_29127255dup , CM000680.1:g.29127253_29127255dup GRCh37
NC_000018.8:g.27381251_27381253dup NCBI36
NG_007072.3:g.54049_54051dup , LRG_397:g.54049_54051dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.*547_*549dup (DSG2) MANE Select ENSP00000261590.8:n.*547_*549dup
ENST00000261590.12:c.*547_*549dup (DSG2) ENSP00000261590.8:n.*547_*549dup
NM_001943.3:c.*547_*549dup , LRG_397t1:c.*547_*549dup (DSG2) NP_001934.2:n.*547_*549dup
NR_045216.1:n.1346-1386_1346-1384dup (DSG2-AS1)
NM_001943.4:c.*547_*549dup (DSG2) NP_001934.2:n.*547_*549dup
XM_024451095.1:c.*547_*549dup (DSG2) XP_024306863.1:n.*547_*549dup
NM_001943.5:c.*547_*549dup (DSG2) MANE Select NP_001934.2:n.*547_*549dup