Canonical Allele Identifier: CA2641408097
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31547483C>A , CM000680.2:g.31547483C>A GRCh38
NC_000018.9:g.29127446C>A , CM000680.1:g.29127446C>A GRCh37
NC_000018.8:g.27381444C>A NCBI36
NG_007072.3:g.54242C>A , LRG_397:g.54242C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.*740C>A (DSG2) MANE Select ENSP00000261590.8:n.*740C>A
ENST00000261590.12:c.*740C>A (DSG2) ENSP00000261590.8:n.*740C>A
NM_001943.3:c.*740C>A , LRG_397t1:c.*740C>A (DSG2) NP_001934.2:n.*740C>A
NR_045216.1:n.1346-1577G>T (DSG2-AS1)
NM_001943.4:c.*740C>A (DSG2) NP_001934.2:n.*740C>A
XM_024451095.1:c.*740C>A (DSG2) XP_024306863.1:n.*740C>A
NM_001943.5:c.*740C>A (DSG2) MANE Select NP_001934.2:n.*740C>A