Canonical Allele Identifier: CA2641407654
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546028_31546030del , CM000680.2:g.31546028_31546030del GRCh38
NC_000018.9:g.29125991_29125993del , CM000680.1:g.29125991_29125993del GRCh37
NC_000018.8:g.27379989_27379991del NCBI36
NG_007072.3:g.52787_52789del , LRG_397:g.52787_52789del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.2642_2644del (DSG2) MANE Select ENSP00000261590.8:p.Thr881_Tyr882delinsAsn
ENST00000261590.12:c.2642_2644del (DSG2) ENSP00000261590.8:p.Thr881_Tyr882delinsAsn
NM_001943.3:c.2642_2644del , LRG_397t1:c.2642_2644del (DSG2) NP_001934.2:p.Thr881_Tyr882delinsAsn
NR_045216.1:n.1346-124_1346-122del (DSG2-AS1)
NM_001943.4:c.2642_2644del (DSG2) NP_001934.2:p.Thr881_Tyr882delinsAsn
XM_024451095.1:c.2108_2110del (DSG2) XP_024306863.1:p.Thr703_Tyr704delinsAsn
NM_001943.5:c.2642_2644del (DSG2) MANE Select NP_001934.2:p.Thr881_Tyr882delinsAsn