Canonical Allele Identifier: CA778425950

Gene: DSG2 DSG2-AS1

Linked Data

• dbSNP Id: rs1170831288
• gnomAD v4: 18-31546958-A-ATC
• MyVariant Identifiers: chr18:g.29126921_29126922insTC (hg19) ; chr18:g.31546958_31546959insTC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31546959_31546960insCT , CM000680.2:g.31546959_31546960insCT	GRCh38
NC_000018.9:g.29126922_29126923insCT , CM000680.1:g.29126922_29126923insCT	GRCh37
NC_000018.8:g.27380920_27380921insCT	NCBI36
NG_007072.3:g.53718_53719insCT , LRG_397:g.53718_53719insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261590.13:c.*216_*217insCT (DSG2) MANE Select	ENSP00000261590.8:n.*216_*217insCT
ENST00000261590.12:c.*216_*217insCT (DSG2)	ENSP00000261590.8:n.*216_*217insCT
NM_001943.3:c.*216_*217insCT , LRG_397t1:c.*216_*217insCT (DSG2)	NP_001934.2:n.*216_*217insCT
NR_045216.1:n.1346-1053_1346-1052insGA (DSG2-AS1)
NM_001943.4:c.*216_*217insCT (DSG2)	NP_001934.2:n.*216_*217insCT
XM_024451095.1:c.*216_*217insCT (DSG2)	XP_024306863.1:n.*216_*217insCT
NM_001943.5:c.*216_*217insCT (DSG2) MANE Select	NP_001934.2:n.*216_*217insCT