Canonical Allele Identifier: CA2293859909
Gene: DSG2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31531419A= , CM000680.2:g.31531419A= GRCh38
NC_000018.9:g.29111382A= , CM000680.1:g.29111382A= GRCh37
NC_000018.8:g.27365380A= NCBI36
NG_007072.3:g.38178A= , LRG_397:g.38178A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000683614.2:n.1278A=
ENST00000683614.1:c.1278A=
ENST00000261590.13:c.1280+167A= MANE Select ENSP00000261590.8:n.1280+167A=
ENST00000261590.12:c.1280+167A= ENSP00000261590.8:n.1280+167A=
NM_001943.3:c.1280+167A= , LRG_397t1:c.1280+167A= NP_001934.2:n.1280+167A=
NM_001943.4:c.1280+167A= NP_001934.2:n.1280+167A=
XM_024451095.1:c.746+167A= XP_024306863.1:n.746+167A=
NM_001943.5:c.1280+167A= MANE Select NP_001934.2:n.1280+167A=
Search 100 bp 5'
Search 100 bp 3'