Canonical Allele Identifier: CA2293859839
Gene: DSG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31531245C= , CM000680.2:g.31531245C= GRCh38
NC_000018.9:g.29111208C= , CM000680.1:g.29111208C= GRCh37
NC_000018.8:g.27365206C= NCBI36
NG_007072.3:g.38004C= , LRG_397:g.38004C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000683614.2:n.1104C=
ENST00000683614.1:c.1104C=
ENST00000261590.13:c.1273C= MANE Select ENSP00000261590.8:p.His425=
ENST00000261590.12:c.1273C= ENSP00000261590.8:p.His425=
NM_001943.3:c.1273C= , LRG_397t1:c.1273C= NP_001934.2:p.His425=
NM_001943.4:c.1273C= NP_001934.2:p.His425=
XM_024451095.1:c.739C= XP_024306863.1:p.His247=
NM_001943.5:c.1273C= MANE Select NP_001934.2:p.His425=