Canonical Allele Identifier: CA2293857218

Gene: DSG2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31524653_31524655delinsCTT , CM000680.2:g.31524653_31524655delinsCTT	GRCh38
NC_000018.9:g.29104616_29104618delinsCTT , CM000680.1:g.29104616_29104618delinsCTT	GRCh37
NC_000018.8:g.27358614_27358616delinsCTT	NCBI36
NG_007072.3:g.31412_31414delinsCTT , LRG_397:g.31412_31414delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682087.2:n.660-50_660-48delinsCTT
ENST00000683614.2:n.660-50_660-48delinsCTT
ENST00000682087.1:c.660-50_660-48delinsCTT
ENST00000683614.1:c.660-50_660-48delinsCTT
ENST00000261590.13:c.829-50_829-48delinsCTT MANE Select	ENSP00000261590.8:n.829-50_829-48delinsCTT
ENST00000261590.12:c.829-50_829-48delinsCTT	ENSP00000261590.8:n.829-50_829-48delinsCTT
NM_001943.3:c.829-50_829-48delinsCTT , LRG_397t1:c.829-50_829-48delinsCTT	NP_001934.2:n.829-50_829-48delinsCTT
NM_001943.4:c.829-50_829-48delinsCTT	NP_001934.2:n.829-50_829-48delinsCTT
XM_024451095.1:c.295-50_295-48delinsCTT	XP_024306863.1:n.295-50_295-48delinsCTT
NM_001943.5:c.829-50_829-48delinsCTT MANE Select	NP_001934.2:n.829-50_829-48delinsCTT