Canonical Allele Identifier: CA778425692

Gene: DSG2 DSG2-AS1

Linked Data

• dbSNP Id: rs1349702462
• MyVariant Identifiers: chr18:g.29126630_29126632del (hg19) ; chr18:g.31546667_31546669del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31546667_31546669del , CM000680.2:g.31546667_31546669del	GRCh38
NC_000018.9:g.29126630_29126632del , CM000680.1:g.29126630_29126632del	GRCh37
NC_000018.8:g.27380628_27380630del	NCBI36
NG_007072.3:g.53426_53428del , LRG_397:g.53426_53428del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261590.13:c.3281_3283del (DSG2) MANE Select	ENSP00000261590.8:p.Gly1094_His1095delinsAsp
ENST00000261590.12:c.3281_3283del (DSG2)	ENSP00000261590.8:p.Gly1094_His1095delinsAsp
NM_001943.3:c.3281_3283del , LRG_397t1:c.3281_3283del (DSG2)	NP_001934.2:p.Gly1094_His1095delinsAsp
NR_045216.1:n.1346-763_1346-761del (DSG2-AS1)
NM_001943.4:c.3281_3283del (DSG2)	NP_001934.2:p.Gly1094_His1095delinsAsp
XM_024451095.1:c.2747_2749del (DSG2)	XP_024306863.1:p.Gly916_His917delinsAsp
NM_001943.5:c.3281_3283del (DSG2) MANE Select	NP_001934.2:p.Gly1094_His1095delinsAsp