Canonical Allele Identifier: CA2293865984
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546026T= , CM000680.2:g.31546026T= GRCh38
NC_000018.9:g.29125989T= , CM000680.1:g.29125989T= GRCh37
NC_000018.8:g.27379987T= NCBI36
NG_007072.3:g.52785T= , LRG_397:g.52785T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.2640T= (DSG2) MANE Select ENSP00000261590.8:p.Asn880=
ENST00000261590.12:c.2640T= (DSG2) ENSP00000261590.8:p.Asn880=
NM_001943.3:c.2640T= , LRG_397t1:c.2640T= (DSG2) NP_001934.2:p.Asn880=
NR_045216.1:n.1346-120A= (DSG2-AS1)
NM_001943.4:c.2640T= (DSG2) NP_001934.2:p.Asn880=
XM_024451095.1:c.2106T= (DSG2) XP_024306863.1:p.Asn702=
NM_001943.5:c.2640T= (DSG2) MANE Select NP_001934.2:p.Asn880=
Search 100 bp 5'
Search 100 bp 3'