Canonical Allele Identifier: CA2641412892
Gene: DSG2 HGNC NCBI

Linked Data

gnomAD v4: 18-31522038-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31522038C>A , CM000680.2:g.31522038C>A GRCh38
NC_000018.9:g.29102001C>A , CM000680.1:g.29102001C>A GRCh37
NC_000018.8:g.27355999C>A NCBI36
NG_007072.3:g.28797C>A , LRG_397:g.28797C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000682087.2:n.355-45C>A
ENST00000682241.2:c.524-45C>A ENSP00000507600.2:n.524-45C>A
ENST00000683614.2:n.355-45C>A
ENST00000682087.1:c.355-45C>A
ENST00000682241.1:c.355-45C>A
ENST00000683614.1:c.355-45C>A
ENST00000683654.1:c.524-45C>A ENSP00000506971.1:n.524-45C>A
ENST00000684461.1:n.1149C>A
ENST00000261590.13:c.524-45C>A MANE Select ENSP00000261590.8:n.524-45C>A
ENST00000261590.12:c.524-45C>A ENSP00000261590.8:n.524-45C>A
ENST00000585206.1:c.524-45C>A ENSP00000462503.1:n.524-45C>A
NM_001943.3:c.524-45C>A , LRG_397t1:c.524-45C>A NP_001934.2:n.524-45C>A
NM_001943.4:c.524-45C>A NP_001934.2:n.524-45C>A
XM_024451095.1:c.-11-45C>A XP_024306863.1:n.-11-45C>A
NM_001943.5:c.524-45C>A MANE Select NP_001934.2:n.524-45C>A
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