Canonical Allele Identifier: CA2641407739
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546902_31546903del , CM000680.2:g.31546902_31546903del GRCh38
NC_000018.9:g.29126865_29126866del , CM000680.1:g.29126865_29126866del GRCh37
NC_000018.8:g.27380863_27380864del NCBI36
NG_007072.3:g.53661_53662del , LRG_397:g.53661_53662del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.*159_*160del (DSG2) MANE Select ENSP00000261590.8:n.*159_*160del
ENST00000261590.12:c.*159_*160del (DSG2) ENSP00000261590.8:n.*159_*160del
NM_001943.3:c.*159_*160del , LRG_397t1:c.*159_*160del (DSG2) NP_001934.2:n.*159_*160del
NR_045216.1:n.1346-996_1346-995del (DSG2-AS1)
NM_001943.4:c.*159_*160del (DSG2) NP_001934.2:n.*159_*160del
XM_024451095.1:c.*159_*160del (DSG2) XP_024306863.1:n.*159_*160del
NM_001943.5:c.*159_*160del (DSG2) MANE Select NP_001934.2:n.*159_*160del