Canonical Allele Identifier: CA2293865991
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546040G= , CM000680.2:g.31546040G= GRCh38
NC_000018.9:g.29126003G= , CM000680.1:g.29126003G= GRCh37
NC_000018.8:g.27380001G= NCBI36
NG_007072.3:g.52799G= , LRG_397:g.52799G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.2654G= (DSG2) MANE Select ENSP00000261590.8:p.Gly885=
ENST00000261590.12:c.2654G= (DSG2) ENSP00000261590.8:p.Gly885=
NM_001943.3:c.2654G= , LRG_397t1:c.2654G= (DSG2) NP_001934.2:p.Gly885=
NR_045216.1:n.1346-134C= (DSG2-AS1)
NM_001943.4:c.2654G= (DSG2) NP_001934.2:p.Gly885=
XM_024451095.1:c.2120G= (DSG2) XP_024306863.1:p.Gly707=
NM_001943.5:c.2654G= (DSG2) MANE Select NP_001934.2:p.Gly885=
Search 100 bp 5'
Search 100 bp 3'