Canonical Allele Identifier: CA402139202
Gene: DSG2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31531177A>C , CM000680.2:g.31531177A>C GRCh38
NC_000018.9:g.29111140A>C , CM000680.1:g.29111140A>C GRCh37
NC_000018.8:g.27365138A>C NCBI36
NG_007072.3:g.37936A>C , LRG_397:g.37936A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000683614.2:n.1036A>C
ENST00000683614.1:c.1036A>C
ENST00000261590.13:c.1205A>C MANE Select ENSP00000261590.8:p.Asp402Ala
ENST00000261590.12:c.1205A>C ENSP00000261590.8:p.Asp402Ala
NM_001943.3:c.1205A>C , LRG_397t1:c.1205A>C NP_001934.2:p.Asp402Ala
NM_001943.4:c.1205A>C NP_001934.2:p.Asp402Ala
XM_024451095.1:c.671A>C XP_024306863.1:p.Asp224Ala
NM_001943.5:c.1205A>C MANE Select NP_001934.2:p.Asp402Ala