Canonical Allele Identifier: CA2293866395
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546894A= , CM000680.2:g.31546894A= GRCh38
NC_000018.9:g.29126857A= , CM000680.1:g.29126857A= GRCh37
NC_000018.8:g.27380855A= NCBI36
NG_007072.3:g.53653A= , LRG_397:g.53653A=

Transcript Alleles

HGVS Amino-acid change
ENST00000261590.13:c.*151A= (DSG2) MANE Select ENSP00000261590.8:n.*151A=
ENST00000261590.12:c.*151A= (DSG2) ENSP00000261590.8:n.*151A=
NM_001943.3:c.*151A= , LRG_397t1:c.*151A= (DSG2) NP_001934.2:n.*151A=
NR_045216.1:n.1346-988T= (DSG2-AS1)
NM_001943.4:c.*151A= (DSG2) NP_001934.2:n.*151A=
XM_024451095.1:c.*151A= (DSG2) XP_024306863.1:n.*151A=
NM_001943.5:c.*151A= (DSG2) MANE Select NP_001934.2:n.*151A=