Canonical Allele Identifier: CA297703066

Gene: DSG2 DSG2-AS1

Linked Data

• dbSNP Id: rs774296097
• MyVariant Identifiers: chr18:g.29127234del (hg19) ; chr18:g.31547271del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31547271del , CM000680.2:g.31547271del	GRCh38
NC_000018.9:g.29127234del , CM000680.1:g.29127234del	GRCh37
NC_000018.8:g.27381232del	NCBI36
NG_007072.3:g.54030del , LRG_397:g.54030del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261590.13:c.*528del (DSG2) MANE Select	ENSP00000261590.8:n.*528del
ENST00000261590.12:c.*528del (DSG2)	ENSP00000261590.8:n.*528del
NM_001943.3:c.*528del , LRG_397t1:c.*528del (DSG2)	NP_001934.2:n.*528del
NR_045216.1:n.1346-1365del (DSG2-AS1)
NM_001943.4:c.*528del (DSG2)	NP_001934.2:n.*528del
XM_024451095.1:c.*528del (DSG2)	XP_024306863.1:n.*528del
NM_001943.5:c.*528del (DSG2) MANE Select	NP_001934.2:n.*528del