Canonical Allele Identifier: CA2293857049
Gene: DSG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31524555T= , CM000680.2:g.31524555T= GRCh38
NC_000018.9:g.29104518T= , CM000680.1:g.29104518T= GRCh37
NC_000018.8:g.27358516T= NCBI36
NG_007072.3:g.31314T= , LRG_397:g.31314T=

Transcript Alleles

HGVS Amino-acid change
ENST00000682087.2:n.629T=
ENST00000683614.2:n.629T=
ENST00000682087.1:c.629T=
ENST00000683614.1:c.629T=
ENST00000261590.13:c.798T= MANE Select ENSP00000261590.8:p.Asn266=
ENST00000261590.12:c.798T= ENSP00000261590.8:p.Asn266=
NM_001943.3:c.798T= , LRG_397t1:c.798T= NP_001934.2:p.Asn266=
NM_001943.4:c.798T= NP_001934.2:p.Asn266=
XM_024451095.1:c.264T= XP_024306863.1:p.Asn88=
NM_001943.5:c.798T= MANE Select NP_001934.2:p.Asn266=