Canonical Allele Identifier: CA402139243
Gene: DSG2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31531181A>T , CM000680.2:g.31531181A>T GRCh38
NC_000018.9:g.29111144A>T , CM000680.1:g.29111144A>T GRCh37
NC_000018.8:g.27365142A>T NCBI36
NG_007072.3:g.37940A>T , LRG_397:g.37940A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000683614.2:n.1040A>T
ENST00000683614.1:c.1040A>T
ENST00000261590.13:c.1209A>T MANE Select ENSP00000261590.8:p.Arg403Ser
ENST00000261590.12:c.1209A>T ENSP00000261590.8:p.Arg403Ser
NM_001943.3:c.1209A>T , LRG_397t1:c.1209A>T NP_001934.2:p.Arg403Ser
NM_001943.4:c.1209A>T NP_001934.2:p.Arg403Ser
XM_024451095.1:c.675A>T XP_024306863.1:p.Arg225Ser
NM_001943.5:c.1209A>T MANE Select NP_001934.2:p.Arg403Ser