Canonical Allele Identifier: CA2293864619
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31542602C= , CM000680.2:g.31542602C= GRCh38
NC_000018.9:g.29122565C= , CM000680.1:g.29122565C= GRCh37
NC_000018.8:g.27376563C= NCBI36
NG_007072.3:g.49361C= , LRG_397:g.49361C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.2084C= (DSG2) MANE Select ENSP00000261590.8:p.Thr695=
ENST00000261590.12:c.2084C= (DSG2) ENSP00000261590.8:p.Thr695=
NM_001943.3:c.2084C= , LRG_397t1:c.2084C= (DSG2) NP_001934.2:p.Thr695=
NR_045216.1:n.1811-281G= (DSG2-AS1)
NM_001943.4:c.2084C= (DSG2) NP_001934.2:p.Thr695=
XM_024451095.1:c.1550C= (DSG2) XP_024306863.1:p.Thr517=
NM_001943.5:c.2084C= (DSG2) MANE Select NP_001934.2:p.Thr695=
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