Canonical Allele Identifier: CA402141500
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31542596A>C , CM000680.2:g.31542596A>C GRCh38
NC_000018.9:g.29122559A>C , CM000680.1:g.29122559A>C GRCh37
NC_000018.8:g.27376557A>C NCBI36
NG_007072.3:g.49355A>C , LRG_397:g.49355A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.2078A>C (DSG2) MANE Select ENSP00000261590.8:p.Glu693Ala
ENST00000261590.12:c.2078A>C (DSG2) ENSP00000261590.8:p.Glu693Ala
NM_001943.3:c.2078A>C , LRG_397t1:c.2078A>C (DSG2) NP_001934.2:p.Glu693Ala
NR_045216.1:n.1811-275T>G (DSG2-AS1)
NM_001943.4:c.2078A>C (DSG2) NP_001934.2:p.Glu693Ala
XM_024451095.1:c.1544A>C (DSG2) XP_024306863.1:p.Glu515Ala
NM_001943.5:c.2078A>C (DSG2) MANE Select NP_001934.2:p.Glu693Ala