Canonical Allele Identifier: CA2641405713
Gene: DSG2 HGNC NCBI

Linked Data

gnomAD v4: 18-31498265-CG-C
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31498268del , CM000680.2:g.31498268del GRCh38
NC_000018.9:g.29078231del , CM000680.1:g.29078231del GRCh37
NC_000018.8:g.27332229del NCBI36
NG_007072.3:g.5027del , LRG_397:g.5027del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682241.2:c.17del ENSP00000507600.2:p.Gly6AspfsTer10
ENST00000683654.1:c.17del ENSP00000506971.1:p.Gly6AspfsTer10
ENST00000261590.13:c.17del MANE Select ENSP00000261590.8:p.Gly6AspfsTer10
ENST00000261590.12:c.17del ENSP00000261590.8:p.Gly6AspfsTer10
ENST00000585206.1:c.17del ENSP00000462503.1:p.Gly6AspfsTer10
NM_001943.3:c.17del , LRG_397t1:c.17del NP_001934.2:p.Gly6AspfsTer10
NM_001943.4:c.17del NP_001934.2:p.Gly6AspfsTer10
NM_001943.5:c.17del MANE Select NP_001934.2:p.Gly6AspfsTer10
Search 100 bp 5'
Search 100 bp 3'