Canonical Allele Identifier: CA2293857280
Gene: DSG2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31524698T= , CM000680.2:g.31524698T= GRCh38
NC_000018.9:g.29104661T= , CM000680.1:g.29104661T= GRCh37
NC_000018.8:g.27358659T= NCBI36
NG_007072.3:g.31457T= , LRG_397:g.31457T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682087.2:n.660-5T=
ENST00000683614.2:n.660-5T=
ENST00000682087.1:c.660-5T=
ENST00000683614.1:c.660-5T=
ENST00000261590.13:c.829-5T= MANE Select ENSP00000261590.8:n.829-5T=
ENST00000261590.12:c.829-5T= ENSP00000261590.8:n.829-5T=
NM_001943.3:c.829-5T= , LRG_397t1:c.829-5T= NP_001934.2:n.829-5T=
NM_001943.4:c.829-5T= NP_001934.2:n.829-5T=
XM_024451095.1:c.295-5T= XP_024306863.1:n.295-5T=
NM_001943.5:c.829-5T= MANE Select NP_001934.2:n.829-5T=
Search 100 bp 5'
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