Canonical Allele Identifier: CA2641407737
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546899A>C , CM000680.2:g.31546899A>C GRCh38
NC_000018.9:g.29126862A>C , CM000680.1:g.29126862A>C GRCh37
NC_000018.8:g.27380860A>C NCBI36
NG_007072.3:g.53658A>C , LRG_397:g.53658A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261590.13:c.*156A>C (DSG2) MANE Select ENSP00000261590.8:n.*156A>C
ENST00000261590.12:c.*156A>C (DSG2) ENSP00000261590.8:n.*156A>C
NM_001943.3:c.*156A>C , LRG_397t1:c.*156A>C (DSG2) NP_001934.2:n.*156A>C
NR_045216.1:n.1346-993T>G (DSG2-AS1)
NM_001943.4:c.*156A>C (DSG2) NP_001934.2:n.*156A>C
XM_024451095.1:c.*156A>C (DSG2) XP_024306863.1:n.*156A>C
NM_001943.5:c.*156A>C (DSG2) MANE Select NP_001934.2:n.*156A>C