Canonical Allele Identifier: CA2293861927
Gene: DSG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31536229C= , CM000680.2:g.31536229C= GRCh38
NC_000018.9:g.29116192C= , CM000680.1:g.29116192C= GRCh37
NC_000018.8:g.27370190C= NCBI36
NG_007072.3:g.42988C= , LRG_397:g.42988C=

Transcript Alleles

HGVS Amino-acid change
ENST00000261590.13:c.1451C= MANE Select ENSP00000261590.8:p.Thr484=
ENST00000261590.12:c.1451C= ENSP00000261590.8:p.Thr484=
NM_001943.3:c.1451C= , LRG_397t1:c.1451C= NP_001934.2:p.Thr484=
NM_001943.4:c.1451C= NP_001934.2:p.Thr484=
XM_024451095.1:c.917C= XP_024306863.1:p.Thr306=
NM_001943.5:c.1451C= MANE Select NP_001934.2:p.Thr484=