Canonical Allele Identifier: CA2293864597
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31542549_31542550delinsAG , CM000680.2:g.31542549_31542550delinsAG GRCh38
NC_000018.9:g.29122512_29122513delinsAG , CM000680.1:g.29122512_29122513delinsAG GRCh37
NC_000018.8:g.27376510_27376511delinsAG NCBI36
NG_007072.3:g.49308_49309delinsAG , LRG_397:g.49308_49309delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.2031_2032delinsAG (DSG2) MANE Select ENSP00000261590.8:p.Gln677=
ENST00000261590.12:c.2031_2032delinsAG (DSG2) ENSP00000261590.8:p.Gln677=
NM_001943.3:c.2031_2032delinsAG , LRG_397t1:c.2031_2032delinsAG (DSG2) NP_001934.2:p.Gln677=
NR_045216.1:n.1811-229_1811-228delinsCT (DSG2-AS1)
NM_001943.4:c.2031_2032delinsAG (DSG2) NP_001934.2:p.Gln677=
XM_024451095.1:c.1497_1498delinsAG (DSG2) XP_024306863.1:p.Gln499=
NM_001943.5:c.2031_2032delinsAG (DSG2) MANE Select NP_001934.2:p.Gln677=