Canonical Allele Identifier: CA2641407267
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31542826_31542828dup , CM000680.2:g.31542826_31542828dup GRCh38
NC_000018.9:g.29122789_29122791dup , CM000680.1:g.29122789_29122791dup GRCh37
NC_000018.8:g.27376787_27376789dup NCBI36
NG_007072.3:g.49585_49587dup , LRG_397:g.49585_49587dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.2308_2310dup (DSG2) MANE Select ENSP00000261590.8:p.Glu770_Phe771insGlu
ENST00000261590.12:c.2308_2310dup (DSG2) ENSP00000261590.8:p.Glu770_Phe771insGlu
NM_001943.3:c.2308_2310dup , LRG_397t1:c.2308_2310dup (DSG2) NP_001934.2:p.Glu770_Phe771insGlu
NR_045216.1:n.1810+277_1810+279dup (DSG2-AS1)
NM_001943.4:c.2308_2310dup (DSG2) NP_001934.2:p.Glu770_Phe771insGlu
XM_024451095.1:c.1774_1776dup (DSG2) XP_024306863.1:p.Glu592_Phe593insGlu
NM_001943.5:c.2308_2310dup (DSG2) MANE Select NP_001934.2:p.Glu770_Phe771insGlu