Canonical Allele Identifier: CA233916
Gene: DPM1 HGNC NCBI
ADNP-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 167008
dbSNP Id: rs727503905

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.50940922T>C , CM000682.2:g.50940922T>C GRCh38
NC_000020.10:g.49557459T>C , CM000682.1:g.49557459T>C GRCh37
NC_000020.9:g.48990866T>C NCBI36
NG_008923.1:g.22602A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371584.9:c.611A>G (DPM1) ENSP00000360640.5:p.Asn204Ser
ENST00000681979.1:n.484A>G (DPM1)
ENST00000682366.1:n.851A>G (DPM1)
ENST00000682713.1:n.1043+1109A>G (DPM1)
ENST00000682754.1:n.610A>G (DPM1)
ENST00000683010.1:n.2235A>G (DPM1)
ENST00000683048.1:c.*78+1109A>G (DPM1) ENSP00000506986.1:n.*78+1109A>G
ENST00000683466.1:c.179+1109A>G (DPM1) ENSP00000507404.1:n.179+1109A>G
ENST00000684193.1:n.1277A>G (DPM1)
ENST00000684708.1:n.541A>G (DPM1)
ENST00000371588.10:c.506A>G (DPM1) MANE Select ENSP00000360644.5:p.Asn169Ser
ENST00000371582.8:c.587A>G (DPM1) ENSP00000360638.4:p.Asn196Ser
ENST00000371584.8:c.609A>G (DPM1)
ENST00000371588.9:c.506A>G (DPM1) ENSP00000360644.5:p.Asn169Ser
ENST00000413082.1:c.491A>G (DPM1) ENSP00000394921.1:p.Asn164Ser
ENST00000466152.5:n.555A>G (DPM1)
ENST00000494752.1:n.276A>G (DPM1)
NM_001317034.1:c.611A>G (DPM1) NP_001303963.1:p.Asn204Ser
NM_001317035.1:c.587A>G (DPM1) NP_001303964.1:p.Asn196Ser
NM_001317036.1:c.494+1109A>G (DPM1) NP_001303965.1:n.494+1109A>G
NM_003859.1:c.506A>G (DPM1) NP_003850.1:p.Asn169Ser
NM_003859.2:c.506A>G (DPM1) NP_003850.1:p.Asn169Ser
NR_110007.1:n.251-3435T>C (ADNP-AS1)
NR_110008.1:n.150-3435T>C (ADNP-AS1)
NR_110009.1:n.147-3435T>C (ADNP-AS1)
NR_133648.1:n.569A>G (DPM1)
XM_011529093.1:c.531A>G (DPM1) XP_011527395.1:p.Gln177=
XR_002958550.1:n.569A>G (DPM1)
XR_002958551.1:n.507+1109A>G (DPM1)
NM_003859.3:c.506A>G (DPM1) MANE Select NP_003850.1:p.Asn169Ser
NR_133648.2:n.537A>G (DPM1)