Canonical Allele Identifier: CA2293861942
Gene: DSG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31536258G= , CM000680.2:g.31536258G= GRCh38
NC_000018.9:g.29116221G= , CM000680.1:g.29116221G= GRCh37
NC_000018.8:g.27370219G= NCBI36
NG_007072.3:g.43017G= , LRG_397:g.43017G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.1480G= MANE Select ENSP00000261590.8:p.Asp494=
ENST00000261590.12:c.1480G= ENSP00000261590.8:p.Asp494=
NM_001943.3:c.1480G= , LRG_397t1:c.1480G= NP_001934.2:p.Asp494=
NM_001943.4:c.1480G= NP_001934.2:p.Asp494=
XM_024451095.1:c.946G= XP_024306863.1:p.Asp316=
NM_001943.5:c.1480G= MANE Select NP_001934.2:p.Asp494=