Canonical Allele Identifier: CA402139159
Gene: DSG2 HGNC NCBI

Linked Data

dbSNP Id: rs2144332994

Genomic Alleles

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

Transcript Alleles

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