Canonical Allele Identifier: CA2293857170

Gene: DSG2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31524601_31524604delinsCTAA , CM000680.2:g.31524601_31524604delinsCTAA	GRCh38
NC_000018.9:g.29104564_29104567delinsCTAA , CM000680.1:g.29104564_29104567delinsCTAA	GRCh37
NC_000018.8:g.27358562_27358565delinsCTAA	NCBI36
NG_007072.3:g.31360_31363delinsCTAA , LRG_397:g.31360_31363delinsCTAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000682087.2:n.659+16_659+19delinsCTAA
ENST00000683614.2:n.659+16_659+19delinsCTAA
ENST00000682087.1:c.659+16_659+19delinsCTAA
ENST00000683614.1:c.659+16_659+19delinsCTAA
ENST00000261590.13:c.828+16_828+19delinsCTAA MANE Select	ENSP00000261590.8:n.828+16_828+19delinsCTAA
ENST00000261590.12:c.828+16_828+19delinsCTAA	ENSP00000261590.8:n.828+16_828+19delinsCTAA
NM_001943.3:c.828+16_828+19delinsCTAA , LRG_397t1:c.828+16_828+19delinsCTAA	NP_001934.2:n.828+16_828+19delinsCTAA
NM_001943.4:c.828+16_828+19delinsCTAA	NP_001934.2:n.828+16_828+19delinsCTAA
XM_024451095.1:c.294+16_294+19delinsCTAA	XP_024306863.1:n.294+16_294+19delinsCTAA
NM_001943.5:c.828+16_828+19delinsCTAA MANE Select	NP_001934.2:n.828+16_828+19delinsCTAA