Canonical Allele Identifier: CA2293854947
Gene: DSG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31519804T= , CM000680.2:g.31519804T= GRCh38
NC_000018.9:g.29099767T= , CM000680.1:g.29099767T= GRCh37
NC_000018.8:g.27353765T= NCBI36
NG_007072.3:g.26563T= , LRG_397:g.26563T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682241.2:c.83T= ENSP00000507600.2:p.Val28=
ENST00000683654.1:c.83T= ENSP00000506971.1:p.Val28=
ENST00000261590.13:c.83T= MANE Select ENSP00000261590.8:p.Val28=
ENST00000261590.12:c.83T= ENSP00000261590.8:p.Val28=
ENST00000585206.1:c.83T= ENSP00000462503.1:p.Val28=
NM_001943.3:c.83T= , LRG_397t1:c.83T= NP_001934.2:p.Val28=
NM_001943.4:c.83T= NP_001934.2:p.Val28=
XM_024451095.1:c.-452T= XP_024306863.1:n.-452T=
NM_001943.5:c.83T= MANE Select NP_001934.2:p.Val28=