Canonical Allele Identifier: CA2293857065
Gene: DSG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31524565C= , CM000680.2:g.31524565C= GRCh38
NC_000018.9:g.29104528C= , CM000680.1:g.29104528C= GRCh37
NC_000018.8:g.27358526C= NCBI36
NG_007072.3:g.31324C= , LRG_397:g.31324C=

Transcript Alleles

HGVS Amino-acid change
ENST00000682087.2:n.639C=
ENST00000683614.2:n.639C=
ENST00000682087.1:c.639C=
ENST00000683614.1:c.639C=
ENST00000261590.13:c.808C= MANE Select ENSP00000261590.8:p.Pro270=
ENST00000261590.12:c.808C= ENSP00000261590.8:p.Pro270=
NM_001943.3:c.808C= , LRG_397t1:c.808C= NP_001934.2:p.Pro270=
NM_001943.4:c.808C= NP_001934.2:p.Pro270=
XM_024451095.1:c.274C= XP_024306863.1:p.Pro92=
NM_001943.5:c.808C= MANE Select NP_001934.2:p.Pro270=