Canonical Allele Identifier: CA339138531

Gene: DHDDS

Linked Data

• ClinVar Variation Id: 1018106
• ClinVar RCV Id: RCV001317360
• dbSNP Id: rs2075180906
• MyVariant Identifiers: chr1:g.26764680A>G (hg19) ; chr1:g.26438189A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26438189A>G , CM000663.2:g.26438189A>G	GRCh38
NC_000001.10:g.26764680A>G , CM000663.1:g.26764680A>G	GRCh37
NC_000001.9:g.26637267A>G	NCBI36
NG_029786.1:g.10908A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528557.6:c.85A>G	ENSP00000515248.1:p.Ile29Val
ENST00000703198.1:c.85A>G	ENSP00000515227.1:p.Ile29Val
ENST00000703199.1:c.85A>G	ENSP00000515228.1:p.Ile29Val
ENST00000703200.1:c.85A>G	ENSP00000515229.1:p.Ile29Val
ENST00000703201.1:c.85A>G	ENSP00000515230.1:p.Ile29Val
ENST00000703202.1:c.85A>G	ENSP00000515231.1:p.Ile29Val
ENST00000703203.1:c.85A>G	ENSP00000515232.1:p.Ile29Val
ENST00000703262.1:c.85A>G	ENSP00000515247.1:p.Ile29Val
ENST00000703263.1:c.85A>G	ENSP00000515249.1:p.Ile29Val
ENST00000236342.12:c.85A>G MANE Select	ENSP00000236342.7:p.Ile29Val
ENST00000236342.11:c.85A>G	ENSP00000236342.7:p.Ile29Val
ENST00000360009.6:c.85A>G	ENSP00000353104.2:p.Ile29Val
ENST00000374185.7:c.85A>G	ENSP00000363300.3:p.Ile29Val
ENST00000374186.7:n.188A>G
ENST00000427245.6:c.85A>G	ENSP00000399177.2:p.Ile29Val
ENST00000430232.5:c.85A>G	ENSP00000397584.1:p.Ile29Val
ENST00000434391.6:c.85A>G	ENSP00000403529.2:p.Ile29Val
ENST00000436153.6:c.85A>G	ENSP00000405604.2:p.Ile29Val
ENST00000487944.5:n.172A>G
ENST00000525165.5:c.85A>G	ENSP00000434185.1:p.Ile29Val
ENST00000525326.5:c.85A>G	ENSP00000431407.1:p.Ile29Val
ENST00000525410.1:n.253A>G
ENST00000525546.5:c.85A>G	ENSP00000433976.1:p.Ile29Val
ENST00000525682.6:c.85A>G	ENSP00000434984.1:p.Ile29Val
ENST00000526219.5:c.85A>G	ENSP00000434219.1:p.Ile29Val
ENST00000526278.5:n.170A>G
ENST00000528557.5:n.262A>G
ENST00000529688.5:n.261A>G
ENST00000530781.5:c.85A>G	ENSP00000433491.1:p.Ile29Val
ENST00000531312.5:c.85A>G	ENSP00000436764.1:p.Ile29Val
ENST00000531955.5:n.305A>G
ENST00000533087.5:c.85A>G	ENSP00000436119.1:p.Ile29Val
NM_001243564.1:c.85A>G	NP_001230493.1:p.Ile29Val
NM_001243565.1:c.85A>G	NP_001230494.1:p.Ile29Val
NM_024887.3:c.85A>G	NP_079163.2:p.Ile29Val
NM_205861.2:c.85A>G	NP_995583.1:p.Ile29Val
XM_006710912.1:c.85A>G	XP_006710975.1:p.Ile29Val
XM_006710913.1:c.85A>G	XP_006710976.1:p.Ile29Val
XM_006710914.1:c.85A>G	XP_006710977.1:p.Ile29Val
XM_006710915.1:c.85A>G	XP_006710978.1:p.Ile29Val
XM_006710916.1:c.-218A>G	XP_006710979.1:n.-218A>G
XM_006710917.1:c.-218A>G	XP_006710980.1:n.-218A>G
XM_006710918.1:c.-218A>G	XP_006710981.1:n.-218A>G
XM_006710919.1:c.-218A>G	XP_006710982.1:n.-218A>G
XM_011542183.1:c.85A>G	XP_011540485.1:p.Ile29Val
XM_011542184.1:c.85A>G	XP_011540486.1:p.Ile29Val
XM_011542185.1:c.85A>G	XP_011540487.1:p.Ile29Val
XM_011542186.1:c.85A>G	XP_011540488.1:p.Ile29Val
NM_001319959.1:c.-218A>G	NP_001306888.1:n.-218A>G
NM_205861.3:c.85A>G MANE Select	NP_995583.1:p.Ile29Val
NM_001243564.2:c.85A>G	NP_001230493.1:p.Ile29Val
NM_001243565.2:c.85A>G	NP_001230494.1:p.Ile29Val
NM_001319959.2:c.-218A>G	NP_001306888.1:n.-218A>G
NM_024887.4:c.85A>G	NP_079163.2:p.Ile29Val