Canonical Allele Identifier: CA2641406226
Gene: DSG2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31524662_31524667del , CM000680.2:g.31524662_31524667del GRCh38
NC_000018.9:g.29104625_29104630del , CM000680.1:g.29104625_29104630del GRCh37
NC_000018.8:g.27358623_27358628del NCBI36
NG_007072.3:g.31421_31426del , LRG_397:g.31421_31426del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682087.2:n.660-41_660-36del
ENST00000683614.2:n.660-41_660-36del
ENST00000682087.1:c.660-41_660-36del
ENST00000683614.1:c.660-41_660-36del
ENST00000261590.13:c.829-41_829-36del MANE Select ENSP00000261590.8:n.829-41_829-36del
ENST00000261590.12:c.829-41_829-36del ENSP00000261590.8:n.829-41_829-36del
NM_001943.3:c.829-41_829-36del , LRG_397t1:c.829-41_829-36del NP_001934.2:n.829-41_829-36del
NM_001943.4:c.829-41_829-36del NP_001934.2:n.829-41_829-36del
XM_024451095.1:c.295-41_295-36del XP_024306863.1:n.295-41_295-36del
NM_001943.5:c.829-41_829-36del MANE Select NP_001934.2:n.829-41_829-36del