Canonical Allele Identifier: CA2641407658
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546699del , CM000680.2:g.31546699del GRCh38
NC_000018.9:g.29126662del , CM000680.1:g.29126662del GRCh37
NC_000018.8:g.27380660del NCBI36
NG_007072.3:g.53458del , LRG_397:g.53458del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.3313del (DSG2) MANE Select ENSP00000261590.8:p.Thr1105ProfsTer22
ENST00000261590.12:c.3313del (DSG2) ENSP00000261590.8:p.Thr1105ProfsTer22
NM_001943.3:c.3313del , LRG_397t1:c.3313del (DSG2) NP_001934.2:p.Thr1105ProfsTer22
NR_045216.1:n.1346-793del (DSG2-AS1)
NM_001943.4:c.3313del (DSG2) NP_001934.2:p.Thr1105ProfsTer22
XM_024451095.1:c.2779del (DSG2) XP_024306863.1:p.Thr927ProfsTer22
NM_001943.5:c.3313del (DSG2) MANE Select NP_001934.2:p.Thr1105ProfsTer22