Canonical Allele Identifier: CA339144912
Community Standard Title: NM_205861.3(DHDDS):c.657+1G>A
Gene: DHDDS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26457906G>A , CM000663.2:g.26457906G>A GRCh38
NC_000001.10:g.26784397G>A , CM000663.1:g.26784397G>A GRCh37
NC_000001.9:g.26656984G>A NCBI36
NG_029786.1:g.30625G>A

Transcript Alleles

HGVS Amino-acid Change
NM_205861.3:c.657+1G>A MANE Select NP_995583.1:n.657+1G>A
ENST00000236342.12:c.657+1G>A MANE Select ENSP00000236342.7:n.657+1G>A
NM_001243564.1:c.555+1G>A NP_001230493.1:n.555+1G>A
NM_001243564.2:c.555+1G>A NP_001230493.1:n.555+1G>A
NM_001243565.1:c.540+1G>A NP_001230494.1:n.540+1G>A
NM_001243565.2:c.540+1G>A NP_001230494.1:n.540+1G>A
NM_001319959.1:c.378+1G>A NP_001306888.1:n.378+1G>A
NM_001319959.2:c.378+1G>A NP_001306888.1:n.378+1G>A
NM_024887.3:c.657+1G>A NP_079163.2:n.657+1G>A
NM_024887.4:c.657+1G>A NP_079163.2:n.657+1G>A
NM_205861.2:c.657+1G>A NP_995583.1:n.657+1G>A
ENST00000236342.11:c.657+1G>A ENSP00000236342.7:n.657+1G>A
ENST00000360009.6:c.657+1G>A ENSP00000353104.2:n.657+1G>A
ENST00000416052.1:c.286+1G>A
ENST00000430232.5:c.540+1G>A ENSP00000397584.1:n.540+1G>A
ENST00000431933.5:c.270+1G>A ENSP00000399781.1:n.270+1G>A
ENST00000434391.6:c.*458+1G>A ENSP00000403529.2:n.*458+1G>A
ENST00000525682.6:c.555+1G>A ENSP00000434984.1:n.555+1G>A
ENST00000526219.5:c.540+1G>A ENSP00000434219.1:n.540+1G>A
ENST00000528557.6:c.657+1G>A ENSP00000515248.1:n.657+1G>A
ENST00000703198.1:c.657+1G>A ENSP00000515227.1:n.657+1G>A
ENST00000703199.1:c.438+1G>A ENSP00000515228.1:n.438+1G>A
ENST00000703200.1:c.*415+1G>A ENSP00000515229.1:n.*415+1G>A
ENST00000703201.1:c.*1603+1G>A ENSP00000515230.1:n.*1603+1G>A
ENST00000703202.1:c.513+1G>A ENSP00000515231.1:n.513+1G>A
ENST00000703203.1:c.*1603+1G>A ENSP00000515232.1:n.*1603+1G>A
ENST00000703262.1:c.657+1G>A ENSP00000515247.1:n.657+1G>A
ENST00000703263.1:c.*188+1G>A ENSP00000515249.1:n.*188+1G>A
ENST00000703264.1:n.985+1G>A
XM_006710912.1:c.657+1G>A XP_006710975.1:n.657+1G>A
XM_006710913.1:c.657+1G>A XP_006710976.1:n.657+1G>A
XM_006710914.1:c.657+1G>A XP_006710977.1:n.657+1G>A
XM_006710915.1:c.555+1G>A XP_006710978.1:n.555+1G>A
XM_006710916.1:c.378+1G>A XP_006710979.1:n.378+1G>A
XM_006710917.1:c.378+1G>A XP_006710980.1:n.378+1G>A
XM_006710918.1:c.378+1G>A XP_006710981.1:n.378+1G>A
XM_006710919.1:c.378+1G>A XP_006710982.1:n.378+1G>A
XM_011542183.1:c.657+1G>A XP_011540485.1:n.657+1G>A
XM_011542184.1:c.657+1G>A XP_011540486.1:n.657+1G>A
XM_011542185.1:c.555+1G>A XP_011540487.1:n.555+1G>A
XM_011542186.1:c.555+1G>A XP_011540488.1:n.555+1G>A