Canonical Allele Identifier: CA402148615
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546517T>A , CM000680.2:g.31546517T>A GRCh38
NC_000018.9:g.29126480T>A , CM000680.1:g.29126480T>A GRCh37
NC_000018.8:g.27380478T>A NCBI36
NG_007072.3:g.53276T>A , LRG_397:g.53276T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.3131T>A (DSG2) MANE Select ENSP00000261590.8:p.Val1044Glu
ENST00000261590.12:c.3131T>A (DSG2) ENSP00000261590.8:p.Val1044Glu
NM_001943.3:c.3131T>A , LRG_397t1:c.3131T>A (DSG2) NP_001934.2:p.Val1044Glu
NR_045216.1:n.1346-611A>T (DSG2-AS1)
NM_001943.4:c.3131T>A (DSG2) NP_001934.2:p.Val1044Glu
XM_024451095.1:c.2597T>A (DSG2) XP_024306863.1:p.Val866Glu
NM_001943.5:c.3131T>A (DSG2) MANE Select NP_001934.2:p.Val1044Glu