Canonical Allele Identifier: CA2293866118
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546292C= , CM000680.2:g.31546292C= GRCh38
NC_000018.9:g.29126255C= , CM000680.1:g.29126255C= GRCh37
NC_000018.8:g.27380253C= NCBI36
NG_007072.3:g.53051C= , LRG_397:g.53051C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.2906C= (DSG2) MANE Select ENSP00000261590.8:p.Ala969=
ENST00000261590.12:c.2906C= (DSG2) ENSP00000261590.8:p.Ala969=
NM_001943.3:c.2906C= , LRG_397t1:c.2906C= (DSG2) NP_001934.2:p.Ala969=
NR_045216.1:n.1346-386G= (DSG2-AS1)
NM_001943.4:c.2906C= (DSG2) NP_001934.2:p.Ala969=
XM_024451095.1:c.2372C= (DSG2) XP_024306863.1:p.Ala791=
NM_001943.5:c.2906C= (DSG2) MANE Select NP_001934.2:p.Ala969=
Search 100 bp 5'
Search 100 bp 3'