Canonical Allele Identifier: CA402148857
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546576C>G , CM000680.2:g.31546576C>G GRCh38
NC_000018.9:g.29126539C>G , CM000680.1:g.29126539C>G GRCh37
NC_000018.8:g.27380537C>G NCBI36
NG_007072.3:g.53335C>G , LRG_397:g.53335C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.3190C>G (DSG2) MANE Select ENSP00000261590.8:p.Pro1064Ala
ENST00000261590.12:c.3190C>G (DSG2) ENSP00000261590.8:p.Pro1064Ala
NM_001943.3:c.3190C>G , LRG_397t1:c.3190C>G (DSG2) NP_001934.2:p.Pro1064Ala
NR_045216.1:n.1346-670G>C (DSG2-AS1)
NM_001943.4:c.3190C>G (DSG2) NP_001934.2:p.Pro1064Ala
XM_024451095.1:c.2656C>G (DSG2) XP_024306863.1:p.Pro886Ala
NM_001943.5:c.3190C>G (DSG2) MANE Select NP_001934.2:p.Pro1064Ala