Canonical Allele Identifier: CA2293864095
Gene: DSG2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31541218C= , CM000680.2:g.31541218C= GRCh38
NC_000018.9:g.29121181C= , CM000680.1:g.29121181C= GRCh37
NC_000018.8:g.27375179C= NCBI36
NG_007072.3:g.47977C= , LRG_397:g.47977C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.1905C= MANE Select ENSP00000261590.8:p.Cys635=
ENST00000261590.12:c.1905C= ENSP00000261590.8:p.Cys635=
NM_001943.3:c.1905C= , LRG_397t1:c.1905C= NP_001934.2:p.Cys635=
NM_001943.4:c.1905C= NP_001934.2:p.Cys635=
XM_024451095.1:c.1371C= XP_024306863.1:p.Cys457=
NM_001943.5:c.1905C= MANE Select NP_001934.2:p.Cys635=
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