Canonical Allele Identifier: CA2293857051
Gene: DSG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31524559A= , CM000680.2:g.31524559A= GRCh38
NC_000018.9:g.29104522A= , CM000680.1:g.29104522A= GRCh37
NC_000018.8:g.27358520A= NCBI36
NG_007072.3:g.31318A= , LRG_397:g.31318A=

Transcript Alleles

HGVS Amino-acid change
ENST00000682087.2:n.633A=
ENST00000683614.2:n.633A=
ENST00000682087.1:c.633A=
ENST00000683614.1:c.633A=
ENST00000261590.13:c.802A= MANE Select ENSP00000261590.8:p.Asn268=
ENST00000261590.12:c.802A= ENSP00000261590.8:p.Asn268=
NM_001943.3:c.802A= , LRG_397t1:c.802A= NP_001934.2:p.Asn268=
NM_001943.4:c.802A= NP_001934.2:p.Asn268=
XM_024451095.1:c.268A= XP_024306863.1:p.Asn90=
NM_001943.5:c.802A= MANE Select NP_001934.2:p.Asn268=