Canonical Allele Identifier: CA2293859823
Gene: DSG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31531196A= , CM000680.2:g.31531196A= GRCh38
NC_000018.9:g.29111159A= , CM000680.1:g.29111159A= GRCh37
NC_000018.8:g.27365157A= NCBI36
NG_007072.3:g.37955A= , LRG_397:g.37955A=

Transcript Alleles

HGVS Amino-acid change
ENST00000683614.2:n.1055A=
ENST00000683614.1:c.1055A=
ENST00000261590.13:c.1224A= MANE Select ENSP00000261590.8:p.Gln408=
ENST00000261590.12:c.1224A= ENSP00000261590.8:p.Gln408=
NM_001943.3:c.1224A= , LRG_397t1:c.1224A= NP_001934.2:p.Gln408=
NM_001943.4:c.1224A= NP_001934.2:p.Gln408=
XM_024451095.1:c.690A= XP_024306863.1:p.Gln230=
NM_001943.5:c.1224A= MANE Select NP_001934.2:p.Gln408=