Canonical Allele Identifier: CA2641406227
Gene: DSG2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31524657_31524668del , CM000680.2:g.31524657_31524668del GRCh38
NC_000018.9:g.29104620_29104631del , CM000680.1:g.29104620_29104631del GRCh37
NC_000018.8:g.27358618_27358629del NCBI36
NG_007072.3:g.31416_31427del , LRG_397:g.31416_31427del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682087.2:n.660-46_660-35del
ENST00000683614.2:n.660-46_660-35del
ENST00000682087.1:c.660-46_660-35del
ENST00000683614.1:c.660-46_660-35del
ENST00000261590.13:c.829-46_829-35del MANE Select ENSP00000261590.8:n.829-46_829-35del
ENST00000261590.12:c.829-46_829-35del ENSP00000261590.8:n.829-46_829-35del
NM_001943.3:c.829-46_829-35del , LRG_397t1:c.829-46_829-35del NP_001934.2:n.829-46_829-35del
NM_001943.4:c.829-46_829-35del NP_001934.2:n.829-46_829-35del
XM_024451095.1:c.295-46_295-35del XP_024306863.1:n.295-46_295-35del
NM_001943.5:c.829-46_829-35del MANE Select NP_001934.2:n.829-46_829-35del