Canonical Allele Identifier: CA402130519
Gene: DSG2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31519809A>C , CM000680.2:g.31519809A>C GRCh38
NC_000018.9:g.29099772A>C , CM000680.1:g.29099772A>C GRCh37
NC_000018.8:g.27353770A>C NCBI36
NG_007072.3:g.26568A>C , LRG_397:g.26568A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682241.2:c.88A>C ENSP00000507600.2:p.Ser30Arg
ENST00000683654.1:c.88A>C ENSP00000506971.1:p.Ser30Arg
ENST00000261590.13:c.88A>C MANE Select ENSP00000261590.8:p.Ser30Arg
ENST00000261590.12:c.88A>C ENSP00000261590.8:p.Ser30Arg
ENST00000585206.1:c.88A>C ENSP00000462503.1:p.Ser30Arg
NM_001943.3:c.88A>C , LRG_397t1:c.88A>C NP_001934.2:p.Ser30Arg
NM_001943.4:c.88A>C NP_001934.2:p.Ser30Arg
XM_024451095.1:c.-447A>C XP_024306863.1:n.-447A>C
NM_001943.5:c.88A>C MANE Select NP_001934.2:p.Ser30Arg