Canonical Allele Identifier: CA2293865934
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31545914A= , CM000680.2:g.31545914A= GRCh38
NC_000018.9:g.29125877A= , CM000680.1:g.29125877A= GRCh37
NC_000018.8:g.27379875A= NCBI36
NG_007072.3:g.52673A= , LRG_397:g.52673A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.2528A= (DSG2) MANE Select ENSP00000261590.8:p.Gln843=
ENST00000261590.12:c.2528A= (DSG2) ENSP00000261590.8:p.Gln843=
NM_001943.3:c.2528A= , LRG_397t1:c.2528A= (DSG2) NP_001934.2:p.Gln843=
NR_045216.1:n.1346-8T= (DSG2-AS1)
NM_001943.4:c.2528A= (DSG2) NP_001934.2:p.Gln843=
XM_024451095.1:c.1994A= (DSG2) XP_024306863.1:p.Gln665=
NM_001943.5:c.2528A= (DSG2) MANE Select NP_001934.2:p.Gln843=