Canonical Allele Identifier: CA2293859820
Gene: DSG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31531189A= , CM000680.2:g.31531189A= GRCh38
NC_000018.9:g.29111152A= , CM000680.1:g.29111152A= GRCh37
NC_000018.8:g.27365150A= NCBI36
NG_007072.3:g.37948A= , LRG_397:g.37948A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000683614.2:n.1048A=
ENST00000683614.1:c.1048A=
ENST00000261590.13:c.1217A= MANE Select ENSP00000261590.8:p.Lys406=
ENST00000261590.12:c.1217A= ENSP00000261590.8:p.Lys406=
NM_001943.3:c.1217A= , LRG_397t1:c.1217A= NP_001934.2:p.Lys406=
NM_001943.4:c.1217A= NP_001934.2:p.Lys406=
XM_024451095.1:c.683A= XP_024306863.1:p.Lys228=
NM_001943.5:c.1217A= MANE Select NP_001934.2:p.Lys406=