Canonical Allele Identifier: CA2293857183

Gene: DSG2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31524614_31524618delinsCTATT , CM000680.2:g.31524614_31524618delinsCTATT	GRCh38
NC_000018.9:g.29104577_29104581delinsCTATT , CM000680.1:g.29104577_29104581delinsCTATT	GRCh37
NC_000018.8:g.27358575_27358579delinsCTATT	NCBI36
NG_007072.3:g.31373_31377delinsCTATT , LRG_397:g.31373_31377delinsCTATT

Transcript Alleles

HGVS	Amino-acid change
ENST00000682087.2:n.659+29_659+33delinsCTATT
ENST00000683614.2:n.659+29_659+33delinsCTATT
ENST00000682087.1:c.659+29_659+33delinsCTATT
ENST00000683614.1:c.659+29_659+33delinsCTATT
ENST00000261590.13:c.828+29_828+33delinsCTATT MANE Select	ENSP00000261590.8:n.828+29_828+33delinsCTATT
ENST00000261590.12:c.828+29_828+33delinsCTATT	ENSP00000261590.8:n.828+29_828+33delinsCTATT
NM_001943.3:c.828+29_828+33delinsCTATT , LRG_397t1:c.828+29_828+33delinsCTATT	NP_001934.2:n.828+29_828+33delinsCTATT
NM_001943.4:c.828+29_828+33delinsCTATT	NP_001934.2:n.828+29_828+33delinsCTATT
XM_024451095.1:c.294+29_294+33delinsCTATT	XP_024306863.1:n.294+29_294+33delinsCTATT
NM_001943.5:c.828+29_828+33delinsCTATT MANE Select	NP_001934.2:n.828+29_828+33delinsCTATT