Canonical Allele Identifier: CA2293859853
Gene: DSG2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31531275T= , CM000680.2:g.31531275T= GRCh38
NC_000018.9:g.29111238T= , CM000680.1:g.29111238T= GRCh37
NC_000018.8:g.27365236T= NCBI36
NG_007072.3:g.38034T= , LRG_397:g.38034T=

Transcript Alleles

HGVS Amino-acid change
ENST00000683614.2:n.1134T=
ENST00000683614.1:c.1134T=
ENST00000261590.13:c.1280+23T= MANE Select ENSP00000261590.8:n.1280+23T=
ENST00000261590.12:c.1280+23T= ENSP00000261590.8:n.1280+23T=
NM_001943.3:c.1280+23T= , LRG_397t1:c.1280+23T= NP_001934.2:n.1280+23T=
NM_001943.4:c.1280+23T= NP_001934.2:n.1280+23T=
XM_024451095.1:c.746+23T= XP_024306863.1:n.746+23T=
NM_001943.5:c.1280+23T= MANE Select NP_001934.2:n.1280+23T=
Search 100 bp 5'
Search 100 bp 3'