Canonical Allele Identifier: CA2293857306
Gene: DSG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31524711G= , CM000680.2:g.31524711G= GRCh38
NC_000018.9:g.29104674G= , CM000680.1:g.29104674G= GRCh37
NC_000018.8:g.27358672G= NCBI36
NG_007072.3:g.31470G= , LRG_397:g.31470G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682087.2:n.668G=
ENST00000683614.2:n.668G=
ENST00000682087.1:c.668G=
ENST00000683614.1:c.668G=
ENST00000261590.13:c.837G= MANE Select ENSP00000261590.8:p.Gly279=
ENST00000261590.12:c.837G= ENSP00000261590.8:p.Gly279=
NM_001943.3:c.837G= , LRG_397t1:c.837G= NP_001934.2:p.Gly279=
NM_001943.4:c.837G= NP_001934.2:p.Gly279=
XM_024451095.1:c.303G= XP_024306863.1:p.Gly101=
NM_001943.5:c.837G= MANE Select NP_001934.2:p.Gly279=