Canonical Allele Identifier: CA2641407822
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31547021A>C , CM000680.2:g.31547021A>C GRCh38
NC_000018.9:g.29126984A>C , CM000680.1:g.29126984A>C GRCh37
NC_000018.8:g.27380982A>C NCBI36
NG_007072.3:g.53780A>C , LRG_397:g.53780A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.*278A>C (DSG2) MANE Select ENSP00000261590.8:n.*278A>C
ENST00000261590.12:c.*278A>C (DSG2) ENSP00000261590.8:n.*278A>C
NM_001943.3:c.*278A>C , LRG_397t1:c.*278A>C (DSG2) NP_001934.2:n.*278A>C
NR_045216.1:n.1346-1115T>G (DSG2-AS1)
NM_001943.4:c.*278A>C (DSG2) NP_001934.2:n.*278A>C
XM_024451095.1:c.*278A>C (DSG2) XP_024306863.1:n.*278A>C
NM_001943.5:c.*278A>C (DSG2) MANE Select NP_001934.2:n.*278A>C