Canonical Allele Identifier: CA2293866159
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546371_31546372delinsTG , CM000680.2:g.31546371_31546372delinsTG GRCh38
NC_000018.9:g.29126334_29126335delinsTG , CM000680.1:g.29126334_29126335delinsTG GRCh37
NC_000018.8:g.27380332_27380333delinsTG NCBI36
NG_007072.3:g.53130_53131delinsTG , LRG_397:g.53130_53131delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.2985_2986delinsTG (DSG2) MANE Select ENSP00000261590.8:p.His995=
ENST00000261590.12:c.2985_2986delinsTG (DSG2) ENSP00000261590.8:p.His995=
NM_001943.3:c.2985_2986delinsTG , LRG_397t1:c.2985_2986delinsTG (DSG2) NP_001934.2:p.His995=
NR_045216.1:n.1346-466_1346-465delinsCA (DSG2-AS1)
NM_001943.4:c.2985_2986delinsTG (DSG2) NP_001934.2:p.His995=
XM_024451095.1:c.2451_2452delinsTG (DSG2) XP_024306863.1:p.His817=
NM_001943.5:c.2985_2986delinsTG (DSG2) MANE Select NP_001934.2:p.His995=