Canonical Allele Identifier: CA402139250
Gene: DSG2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31531183C>T , CM000680.2:g.31531183C>T GRCh38
NC_000018.9:g.29111146C>T , CM000680.1:g.29111146C>T GRCh37
NC_000018.8:g.27365144C>T NCBI36
NG_007072.3:g.37942C>T , LRG_397:g.37942C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000683614.2:n.1042C>T
ENST00000683614.1:c.1042C>T
ENST00000261590.13:c.1211C>T MANE Select ENSP00000261590.8:p.Ser404Leu
ENST00000261590.12:c.1211C>T ENSP00000261590.8:p.Ser404Leu
NM_001943.3:c.1211C>T , LRG_397t1:c.1211C>T NP_001934.2:p.Ser404Leu
NM_001943.4:c.1211C>T NP_001934.2:p.Ser404Leu
XM_024451095.1:c.677C>T XP_024306863.1:p.Ser226Leu
NM_001943.5:c.1211C>T MANE Select NP_001934.2:p.Ser404Leu