Canonical Allele Identifier: CA2293855890
Gene: DSG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31522189G= , CM000680.2:g.31522189G= GRCh38
NC_000018.9:g.29102152G= , CM000680.1:g.29102152G= GRCh37
NC_000018.8:g.27356150G= NCBI36
NG_007072.3:g.28948G= , LRG_397:g.28948G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682087.2:n.461G=
ENST00000682241.2:c.630G= ENSP00000507600.2:p.Val210=
ENST00000683614.2:n.461G=
ENST00000682087.1:c.461G=
ENST00000682241.1:c.461G=
ENST00000683614.1:c.461G=
ENST00000683654.1:c.630G= ENSP00000506971.1:p.Val210=
ENST00000684461.1:n.1300G=
ENST00000261590.13:c.630G= MANE Select ENSP00000261590.8:p.Val210=
ENST00000261590.12:c.630G= ENSP00000261590.8:p.Val210=
ENST00000585206.1:c.630G= ENSP00000462503.1:p.Val210=
NM_001943.3:c.630G= , LRG_397t1:c.630G= NP_001934.2:p.Val210=
NM_001943.4:c.630G= NP_001934.2:p.Val210=
XM_024451095.1:c.96G= XP_024306863.1:p.Val32=
NM_001943.5:c.630G= MANE Select NP_001934.2:p.Val210=