Canonical Allele Identifier: CA2293856943
Gene: DSG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31524776T= , CM000680.2:g.31524776T= GRCh38
NC_000018.9:g.29104739T= , CM000680.1:g.29104739T= GRCh37
NC_000018.8:g.27358737T= NCBI36
NG_007072.3:g.31535T= , LRG_397:g.31535T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682087.2:n.733T=
ENST00000683614.2:n.733T=
ENST00000682087.1:c.733T=
ENST00000683614.1:c.733T=
ENST00000261590.13:c.902T= MANE Select ENSP00000261590.8:p.Ile301=
ENST00000261590.12:c.902T= ENSP00000261590.8:p.Ile301=
NM_001943.3:c.902T= , LRG_397t1:c.902T= NP_001934.2:p.Ile301=
NM_001943.4:c.902T= NP_001934.2:p.Ile301=
XM_024451095.1:c.368T= XP_024306863.1:p.Ile123=
NM_001943.5:c.902T= MANE Select NP_001934.2:p.Ile301=