Canonical Allele Identifier: CA2293866575
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31547304T= , CM000680.2:g.31547304T= GRCh38
NC_000018.9:g.29127267T= , CM000680.1:g.29127267T= GRCh37
NC_000018.8:g.27381265T= NCBI36
NG_007072.3:g.54063T= , LRG_397:g.54063T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.*561T= (DSG2) MANE Select ENSP00000261590.8:n.*561T=
ENST00000261590.12:c.*561T= (DSG2) ENSP00000261590.8:n.*561T=
NM_001943.3:c.*561T= , LRG_397t1:c.*561T= (DSG2) NP_001934.2:n.*561T=
NR_045216.1:n.1346-1398A= (DSG2-AS1)
NM_001943.4:c.*561T= (DSG2) NP_001934.2:n.*561T=
XM_024451095.1:c.*561T= (DSG2) XP_024306863.1:n.*561T=
NM_001943.5:c.*561T= (DSG2) MANE Select NP_001934.2:n.*561T=