Canonical Allele Identifier: CA2293855454
Gene: DSG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31521134T= , CM000680.2:g.31521134T= GRCh38
NC_000018.9:g.29101097T= , CM000680.1:g.29101097T= GRCh37
NC_000018.8:g.27355095T= NCBI36
NG_007072.3:g.27893T= , LRG_397:g.27893T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682087.2:n.245T=
ENST00000682241.2:c.414T= ENSP00000507600.2:p.Asn138=
ENST00000683614.2:n.245T=
ENST00000682087.1:c.245T=
ENST00000682241.1:c.245T=
ENST00000683614.1:c.245T=
ENST00000683654.1:c.414T= ENSP00000506971.1:p.Asn138=
ENST00000684461.1:n.245T=
ENST00000261590.13:c.414T= MANE Select ENSP00000261590.8:p.Asn138=
ENST00000261590.12:c.414T= ENSP00000261590.8:p.Asn138=
ENST00000585206.1:c.414T= ENSP00000462503.1:p.Asn138=
NM_001943.3:c.414T= , LRG_397t1:c.414T= NP_001934.2:p.Asn138=
NM_001943.4:c.414T= NP_001934.2:p.Asn138=
XM_024451095.1:c.-121T= XP_024306863.1:n.-121T=
NM_001943.5:c.414T= MANE Select NP_001934.2:p.Asn138=