Canonical Allele Identifier: CA116050
Gene: DYM HGNC NCBI

Linked Data

ClinVar Variation Id: 3189
dbSNP Id: rs120074164

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.49379693C>T , CM000680.2:g.49379693C>T GRCh38
NC_000018.9:g.46906063C>T , CM000680.1:g.46906063C>T GRCh37
NC_000018.8:g.45160061C>T NCBI36
NG_009239.1:g.86017G>A
NG_009239.2:g.86041G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000675505.1:c.259G>A MANE Select ENSP00000501694.1:p.Glu87Lys
ENST00000269445.10:c.259G>A ENSP00000269445.6:p.Glu87Lys
ENST00000418472.6:c.-20G>A ENSP00000415292.2:n.-20G>A
ENST00000442713.6:c.193+11900G>A ENSP00000395942.2:n.193+11900G>A
ENST00000578596.5:n.383G>A
ENST00000579058.5:c.*255G>A ENSP00000462954.1:n.*255G>A
ENST00000583353.1:c.259G>A ENSP00000464089.1:p.Glu87Lys
NM_017653.3:c.259G>A NP_060123.3:p.Glu87Lys
XM_006722488.2:c.259G>A XP_006722551.1:p.Glu87Lys
XM_006722490.2:c.259G>A XP_006722553.1:p.Glu87Lys
XM_006722491.1:c.259G>A XP_006722554.1:p.Glu87Lys
XM_006722492.2:c.259G>A XP_006722555.1:p.Glu87Lys
XM_011526036.1:c.259G>A XP_011524338.1:p.Glu87Lys
XM_011526037.1:c.256G>A XP_011524339.1:p.Glu86Lys
XM_011526038.1:c.259G>A XP_011524340.1:p.Glu87Lys
XM_011526039.1:c.259G>A XP_011524341.1:p.Glu87Lys
XM_011526040.1:c.91G>A XP_011524342.1:p.Glu31Lys
XM_011526041.1:c.259G>A XP_011524343.1:p.Glu87Lys
XM_011526042.1:c.259G>A XP_011524344.1:p.Glu87Lys
XM_011526043.1:c.259G>A XP_011524345.1:p.Glu87Lys
NM_001353210.1:c.259G>A NP_001340139.1:p.Glu87Lys
NM_001353211.1:c.256G>A NP_001340140.1:p.Glu86Lys
NM_001353212.1:c.256G>A NP_001340141.1:p.Glu86Lys
NM_001353213.1:c.259G>A NP_001340142.1:p.Glu87Lys
NM_001353214.1:c.259G>A NP_001340143.1:p.Glu87Lys
NM_001353215.1:c.259G>A NP_001340144.1:p.Glu87Lys
NM_001353216.1:c.259G>A NP_001340145.1:p.Glu87Lys
NM_017653.4:c.259G>A NP_060123.3:p.Glu87Lys
XM_006722488.3:c.259G>A XP_006722551.1:p.Glu87Lys
XM_006722492.4:c.259G>A XP_006722555.1:p.Glu87Lys
XM_011526036.2:c.259G>A XP_011524338.1:p.Glu87Lys
XM_011526038.2:c.259G>A XP_011524340.1:p.Glu87Lys
XM_011526039.2:c.259G>A XP_011524341.1:p.Glu87Lys
XM_011526041.2:c.259G>A XP_011524343.1:p.Glu87Lys
XM_011526042.2:c.259G>A XP_011524344.1:p.Glu87Lys
XM_017025795.1:c.256G>A XP_016881284.1:p.Glu86Lys
XM_017025796.2:c.79G>A XP_016881285.1:p.Glu27Lys
XM_017025800.2:c.259G>A XP_016881289.1:p.Glu87Lys
XM_017025801.1:c.256G>A XP_016881290.1:p.Glu86Lys
XR_002958177.1:n.616G>A
NM_001353210.3:c.259G>A NP_001340139.1:p.Glu87Lys
NM_001353211.3:c.256G>A NP_001340140.1:p.Glu86Lys
NM_001353212.3:c.256G>A NP_001340141.1:p.Glu86Lys
NM_001353213.3:c.259G>A NP_001340142.1:p.Glu87Lys
NM_001353214.3:c.259G>A MANE Select NP_001340143.1:p.Glu87Lys
NM_001353215.3:c.259G>A NP_001340144.1:p.Glu87Lys
NM_001353216.3:c.259G>A NP_001340145.1:p.Glu87Lys
NM_001374428.1:c.259G>A NP_001361357.1:p.Glu87Lys
NM_001374429.1:c.256G>A NP_001361358.1:p.Glu86Lys
NM_001374430.1:c.259G>A NP_001361359.1:p.Glu87Lys
NM_001374431.1:c.259G>A NP_001361360.1:p.Glu87Lys
NM_001374432.1:c.259G>A NP_001361361.1:p.Glu87Lys
NM_001374433.1:c.259G>A NP_001361362.1:p.Glu87Lys
NM_001374434.1:c.259G>A NP_001361363.1:p.Glu87Lys
NM_001374435.1:c.259G>A NP_001361364.1:p.Glu87Lys
NM_001374436.1:c.259G>A NP_001361365.1:p.Glu87Lys
NM_001374437.1:c.259G>A NP_001361366.1:p.Glu87Lys
NM_001374438.1:c.259G>A NP_001361367.1:p.Glu87Lys
NM_001374439.1:c.256G>A NP_001361368.1:p.Glu86Lys
NM_001374440.1:c.193+11900G>A NP_001361369.1:n.193+11900G>A
NM_001374441.1:c.193+11900G>A NP_001361370.1:n.193+11900G>A
NM_001374442.1:c.193+11900G>A NP_001361371.1:n.193+11900G>A
NM_001374443.1:c.193+11900G>A NP_001361372.1:n.193+11900G>A
NM_001374444.1:c.193+11900G>A NP_001361373.1:n.193+11900G>A
NM_017653.6:c.259G>A NP_060123.3:p.Glu87Lys