Canonical Allele Identifier: CA2293856867
Gene: DSG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31524752T= , CM000680.2:g.31524752T= GRCh38
NC_000018.9:g.29104715T= , CM000680.1:g.29104715T= GRCh37
NC_000018.8:g.27358713T= NCBI36
NG_007072.3:g.31511T= , LRG_397:g.31511T=

Transcript Alleles

HGVS Amino-acid change
ENST00000682087.2:n.709T=
ENST00000683614.2:n.709T=
ENST00000682087.1:c.709T=
ENST00000683614.1:c.709T=
ENST00000261590.13:c.878T= MANE Select ENSP00000261590.8:p.Ile293=
ENST00000261590.12:c.878T= ENSP00000261590.8:p.Ile293=
NM_001943.3:c.878T= , LRG_397t1:c.878T= NP_001934.2:p.Ile293=
NM_001943.4:c.878T= NP_001934.2:p.Ile293=
XM_024451095.1:c.344T= XP_024306863.1:p.Ile115=
NM_001943.5:c.878T= MANE Select NP_001934.2:p.Ile293=