Canonical Allele Identifier: CA402139157
Gene: DSG2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31531172C>G , CM000680.2:g.31531172C>G GRCh38
NC_000018.9:g.29111135C>G , CM000680.1:g.29111135C>G GRCh37
NC_000018.8:g.27365133C>G NCBI36
NG_007072.3:g.37931C>G , LRG_397:g.37931C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000683614.2:n.1031C>G
ENST00000683614.1:c.1031C>G
ENST00000261590.13:c.1200C>G MANE Select ENSP00000261590.8:p.Ser400Arg
ENST00000261590.12:c.1200C>G ENSP00000261590.8:p.Ser400Arg
NM_001943.3:c.1200C>G , LRG_397t1:c.1200C>G NP_001934.2:p.Ser400Arg
NM_001943.4:c.1200C>G NP_001934.2:p.Ser400Arg
XM_024451095.1:c.666C>G XP_024306863.1:p.Ser222Arg
NM_001943.5:c.1200C>G MANE Select NP_001934.2:p.Ser400Arg