Canonical Allele Identifier: CA402147438
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546322A>G , CM000680.2:g.31546322A>G GRCh38
NC_000018.9:g.29126285A>G , CM000680.1:g.29126285A>G GRCh37
NC_000018.8:g.27380283A>G NCBI36
NG_007072.3:g.53081A>G , LRG_397:g.53081A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261590.13:c.2936A>G (DSG2) MANE Select ENSP00000261590.8:p.Tyr979Cys
ENST00000261590.12:c.2936A>G (DSG2) ENSP00000261590.8:p.Tyr979Cys
NM_001943.3:c.2936A>G , LRG_397t1:c.2936A>G (DSG2) NP_001934.2:p.Tyr979Cys
NR_045216.1:n.1346-416T>C (DSG2-AS1)
NM_001943.4:c.2936A>G (DSG2) NP_001934.2:p.Tyr979Cys
XM_024451095.1:c.2402A>G (DSG2) XP_024306863.1:p.Tyr801Cys
NM_001943.5:c.2936A>G (DSG2) MANE Select NP_001934.2:p.Tyr979Cys