Canonical Allele Identifier: CA2293857197

Gene: DSG2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31524645_31524646delinsAT , CM000680.2:g.31524645_31524646delinsAT	GRCh38
NC_000018.9:g.29104608_29104609delinsAT , CM000680.1:g.29104608_29104609delinsAT	GRCh37
NC_000018.8:g.27358606_27358607delinsAT	NCBI36
NG_007072.3:g.31404_31405delinsAT , LRG_397:g.31404_31405delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682087.2:n.660-58_660-57delinsAT
ENST00000683614.2:n.660-58_660-57delinsAT
ENST00000682087.1:c.660-58_660-57delinsAT
ENST00000683614.1:c.660-58_660-57delinsAT
ENST00000261590.13:c.829-58_829-57delinsAT MANE Select	ENSP00000261590.8:n.829-58_829-57delinsAT
ENST00000261590.12:c.829-58_829-57delinsAT	ENSP00000261590.8:n.829-58_829-57delinsAT
NM_001943.3:c.829-58_829-57delinsAT , LRG_397t1:c.829-58_829-57delinsAT	NP_001934.2:n.829-58_829-57delinsAT
NM_001943.4:c.829-58_829-57delinsAT	NP_001934.2:n.829-58_829-57delinsAT
XM_024451095.1:c.295-58_295-57delinsAT	XP_024306863.1:n.295-58_295-57delinsAT
NM_001943.5:c.829-58_829-57delinsAT MANE Select	NP_001934.2:n.829-58_829-57delinsAT