Canonical Allele Identifier: CA2293861976
Gene: DSG2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31536333G= , CM000680.2:g.31536333G= GRCh38
NC_000018.9:g.29116296G= , CM000680.1:g.29116296G= GRCh37
NC_000018.8:g.27370294G= NCBI36
NG_007072.3:g.43092G= , LRG_397:g.43092G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.1555G= MANE Select ENSP00000261590.8:p.Asp519=
ENST00000261590.12:c.1555G= ENSP00000261590.8:p.Asp519=
NM_001943.3:c.1555G= , LRG_397t1:c.1555G= NP_001934.2:p.Asp519=
NM_001943.4:c.1555G= NP_001934.2:p.Asp519=
XM_024451095.1:c.1021G= XP_024306863.1:p.Asp341=
NM_001943.5:c.1555G= MANE Select NP_001934.2:p.Asp519=
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