Canonical Allele Identifier: CA2293859822
Gene: DSG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31531193C= , CM000680.2:g.31531193C= GRCh38
NC_000018.9:g.29111156C= , CM000680.1:g.29111156C= GRCh37
NC_000018.8:g.27365154C= NCBI36
NG_007072.3:g.37952C= , LRG_397:g.37952C=

Transcript Alleles

HGVS Amino-acid change
ENST00000683614.2:n.1052C=
ENST00000683614.1:c.1052C=
ENST00000261590.13:c.1221C= MANE Select ENSP00000261590.8:p.Gly407=
ENST00000261590.12:c.1221C= ENSP00000261590.8:p.Gly407=
NM_001943.3:c.1221C= , LRG_397t1:c.1221C= NP_001934.2:p.Gly407=
NM_001943.4:c.1221C= NP_001934.2:p.Gly407=
XM_024451095.1:c.687C= XP_024306863.1:p.Gly229=
NM_001943.5:c.1221C= MANE Select NP_001934.2:p.Gly407=