Canonical Allele Identifier: CA402148514
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546501G>T , CM000680.2:g.31546501G>T GRCh38
NC_000018.9:g.29126464G>T , CM000680.1:g.29126464G>T GRCh37
NC_000018.8:g.27380462G>T NCBI36
NG_007072.3:g.53260G>T , LRG_397:g.53260G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261590.13:c.3115G>T (DSG2) MANE Select ENSP00000261590.8:p.Ala1039Ser
ENST00000261590.12:c.3115G>T ENSP00000261590.8:p.Ala1039Ser
NM_001943.3:c.3115G>T , LRG_397t1:c.3115G>T (DSG2) NP_001934.2:p.Ala1039Ser
NR_045216.1:n.1346-595C>A (DSG2-AS1)
NM_001943.4:c.3115G>T (DSG2) NP_001934.2:p.Ala1039Ser
XM_024451095.1:c.2581G>T (DSG2) XP_024306863.1:p.Ala861Ser
NM_001943.5:c.3115G>T (DSG2) MANE Select NP_001934.2:p.Ala1039Ser