Canonical Allele Identifier: CA297722906
Gene: DSG4 HGNC NCBI
DSG1-AS1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31376779C>T , CM000680.2:g.31376779C>T GRCh38
NC_000018.9:g.28956742C>T , CM000680.1:g.28956742C>T GRCh37
NC_000018.8:g.27210740C>T NCBI36
NG_013040.1:g.5003C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000308128.9:c.-133C>T (DSG4) MANE Select ENSP00000311859.4:n.-133C>T
ENST00000308128.8:c.-133C>T (DSG4) ENSP00000311859.4:n.-133C>T
NM_001134453.1:c.-133C>T (DSG4) NP_001127925.1:n.-133C>T
NM_177986.3:c.-133C>T (DSG4) NP_817123.1:n.-133C>T
NR_110788.1:n.157-22326G>A (DSG1-AS1)
NM_001134453.2:c.-133C>T (DSG4) NP_001127925.1:n.-133C>T
NM_177986.4:c.-133C>T (DSG4) NP_817123.1:n.-133C>T
NM_177986.5:c.-133C>T (DSG4) MANE Select NP_817123.1:n.-133C>T
NM_001134453.3:c.-133C>T (DSG4) NP_001127925.1:n.-133C>T