Canonical Allele Identifier: CA339145513

Gene: DHDDS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26468901C>T , CM000663.2:g.26468901C>T	GRCh38
NC_000001.10:g.26795392C>T , CM000663.1:g.26795392C>T	GRCh37
NC_000001.9:g.26667979C>T	NCBI36
NG_029786.1:g.41620C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528557.6:c.772C>T	ENSP00000515248.1:p.Arg258Ter
ENST00000703198.1:c.664C>T	ENSP00000515227.1:p.Arg222Ter
ENST00000703199.1:c.553C>T	ENSP00000515228.1:p.Arg185Ter
ENST00000703200.1:c.*530C>T	ENSP00000515229.1:n.*530C>T
ENST00000703201.1:c.*1721C>T	ENSP00000515230.1:n.*1721C>T
ENST00000703202.1:c.628C>T	ENSP00000515231.1:p.Arg210Ter
ENST00000703203.1:c.*1718C>T	ENSP00000515232.1:n.*1718C>T
ENST00000703262.1:c.869C>T	ENSP00000515247.1:p.Pro290Leu
ENST00000703263.1:c.*303C>T	ENSP00000515249.1:n.*303C>T
ENST00000236342.12:c.772C>T MANE Select	ENSP00000236342.7:p.Arg258Ter
ENST00000236342.11:c.772C>T	ENSP00000236342.7:p.Arg258Ter
ENST00000360009.6:c.775C>T	ENSP00000353104.2:p.Arg259Ter
ENST00000431933.5:c.280C>T	ENSP00000399781.1:p.Arg94Ter
ENST00000434391.6:c.*573C>T	ENSP00000403529.2:n.*573C>T
ENST00000525682.6:c.670C>T	ENSP00000434984.1:p.Arg224Ter
ENST00000526219.5:c.655C>T	ENSP00000434219.1:p.Arg219Ter
NM_001243564.1:c.670C>T	NP_001230493.1:p.Arg224Ter
NM_001243565.1:c.655C>T	NP_001230494.1:p.Arg219Ter
NM_024887.3:c.775C>T	NP_079163.2:p.Arg259Ter
NM_205861.2:c.772C>T	NP_995583.1:p.Arg258Ter
XM_006710912.1:c.775C>T	XP_006710975.1:p.Arg259Ter
XM_006710913.1:c.775C>T	XP_006710976.1:p.Arg259Ter
XM_006710914.1:c.775C>T	XP_006710977.1:p.Arg259Ter
XM_006710915.1:c.673C>T	XP_006710978.1:p.Arg225Ter
XM_006710916.1:c.496C>T	XP_006710979.1:p.Arg166Ter
XM_006710917.1:c.496C>T	XP_006710980.1:p.Arg166Ter
XM_006710918.1:c.496C>T	XP_006710981.1:p.Arg166Ter
XM_006710919.1:c.493C>T	XP_006710982.1:p.Arg165Ter
XM_011542183.1:c.775C>T	XP_011540485.1:p.Arg259Ter
XM_011542184.1:c.772C>T	XP_011540486.1:p.Arg258Ter
XM_011542185.1:c.673C>T	XP_011540487.1:p.Arg225Ter
XM_011542186.1:c.670C>T	XP_011540488.1:p.Arg224Ter
NM_001319959.1:c.493C>T	NP_001306888.1:p.Arg165Ter
NM_205861.3:c.772C>T MANE Select	NP_995583.1:p.Arg258Ter
NM_001243564.2:c.670C>T	NP_001230493.1:p.Arg224Ter
NM_001243565.2:c.655C>T	NP_001230494.1:p.Arg219Ter
NM_001319959.2:c.493C>T	NP_001306888.1:p.Arg165Ter
NM_024887.4:c.775C>T	NP_079163.2:p.Arg259Ter