Canonical Allele Identifier: CA2641407886
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31547171_31547183del , CM000680.2:g.31547171_31547183del GRCh38
NC_000018.9:g.29127134_29127146del , CM000680.1:g.29127134_29127146del GRCh37
NC_000018.8:g.27381132_27381144del NCBI36
NG_007072.3:g.53930_53942del , LRG_397:g.53930_53942del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.*428_*440del (DSG2) MANE Select ENSP00000261590.8:n.*428_*440del
ENST00000261590.12:c.*428_*440del (DSG2) ENSP00000261590.8:n.*428_*440del
NM_001943.3:c.*428_*440del , LRG_397t1:c.*428_*440del (DSG2) NP_001934.2:n.*428_*440del
NR_045216.1:n.1346-1277_1346-1265del (DSG2-AS1)
NM_001943.4:c.*428_*440del (DSG2) NP_001934.2:n.*428_*440del
XM_024451095.1:c.*428_*440del (DSG2) XP_024306863.1:n.*428_*440del
NM_001943.5:c.*428_*440del (DSG2) MANE Select NP_001934.2:n.*428_*440del