Canonical Allele Identifier: CA2641412891
Gene: DSG2 HGNC NCBI

Linked Data

gnomAD v4: 18-31522030-TA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31522033del , CM000680.2:g.31522033del GRCh38
NC_000018.9:g.29101996del , CM000680.1:g.29101996del GRCh37
NC_000018.8:g.27355994del NCBI36
NG_007072.3:g.28792del , LRG_397:g.28792del

Transcript Alleles

HGVS Amino-acid change
ENST00000682087.2:n.355-50del
ENST00000682241.2:c.524-50del ENSP00000507600.2:n.524-50del
ENST00000683614.2:n.355-50del
ENST00000682087.1:c.355-50del
ENST00000682241.1:c.355-50del
ENST00000683614.1:c.355-50del
ENST00000683654.1:c.524-50del ENSP00000506971.1:n.524-50del
ENST00000684461.1:n.1144del
ENST00000261590.13:c.524-50del MANE Select ENSP00000261590.8:n.524-50del
ENST00000261590.12:c.524-50del ENSP00000261590.8:n.524-50del
ENST00000585206.1:c.524-50del ENSP00000462503.1:n.524-50del
NM_001943.3:c.524-50del , LRG_397t1:c.524-50del NP_001934.2:n.524-50del
NM_001943.4:c.524-50del NP_001934.2:n.524-50del
XM_024451095.1:c.-11-50del XP_024306863.1:n.-11-50del
NM_001943.5:c.524-50del MANE Select NP_001934.2:n.524-50del
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