Canonical Allele Identifier: CA2293859911
Gene: DSG2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31531423G= , CM000680.2:g.31531423G= GRCh38
NC_000018.9:g.29111386G= , CM000680.1:g.29111386G= GRCh37
NC_000018.8:g.27365384G= NCBI36
NG_007072.3:g.38182G= , LRG_397:g.38182G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000683614.2:n.1282G=
ENST00000683614.1:c.1282G=
ENST00000261590.13:c.1280+171G= MANE Select ENSP00000261590.8:n.1280+171G=
ENST00000261590.12:c.1280+171G= ENSP00000261590.8:n.1280+171G=
NM_001943.3:c.1280+171G= , LRG_397t1:c.1280+171G= NP_001934.2:n.1280+171G=
NM_001943.4:c.1280+171G= NP_001934.2:n.1280+171G=
XM_024451095.1:c.746+171G= XP_024306863.1:n.746+171G=
NM_001943.5:c.1280+171G= MANE Select NP_001934.2:n.1280+171G=
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