Canonical Allele Identifier: CA152574
Gene: DLAT HGNC NCBI

Linked Data

ClinVar Variation Id: 128897
dbSNP Id: rs2303436

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112025600C>T , CM000673.2:g.112025600C>T GRCh38
NC_000011.9:g.111896324C>T , CM000673.1:g.111896324C>T GRCh37
NC_000011.8:g.111401534C>T NCBI36
NG_013342.1:g.5787C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000280346.11:c.128C>T MANE Select ENSP00000280346.7:p.Ala43Val
ENST00000531306.2:c.128C>T ENSP00000433432.2:p.Ala43Val
ENST00000679368.1:c.128C>T ENSP00000505314.1:p.Ala43Val
ENST00000679614.1:c.24+104C>T ENSP00000506007.1:p.=
ENST00000679815.1:c.128C>T ENSP00000504880.1:p.Ala43Val
ENST00000679878.1:c.128C>T ENSP00000505567.1:p.Ala43Val
ENST00000680010.1:c.128C>T ENSP00000505768.1:p.Ala43Val
ENST00000680331.1:c.128C>T ENSP00000506707.1:p.Ala43Val
ENST00000681316.1:c.128C>T ENSP00000506560.1:p.Ala43Val
ENST00000681328.1:c.128C>T ENSP00000506355.1:p.Ala43Val
ENST00000681339.1:c.128C>T ENSP00000506167.1:p.Ala43Val
ENST00000681638.1:c.128C>T ENSP00000506090.1:p.Ala43Val
ENST00000280346.10:c.128C>T ENSP00000280346.6:p.Ala43Val
ENST00000393051.5:c.128C>T ENSP00000376771.1:p.Ala43Val
ENST00000531306.1:n.5C>T ENSP00000433432.1:p.Ala2Val
ENST00000533297.1:c.128C>T ENSP00000435374.1:p.Ala43Val
NM_001931.4:c.128C>T NP_001922.2:p.Ala43Val
XM_011542647.1:c.128C>T XP_011540949.1:p.Ala43Val
XM_011542647.3:c.128C>T XP_011540949.1:p.Ala43Val
NM_001372031.1:c.128C>T NP_001358960.1:p.Ala43Val
NM_001372032.1:c.128C>T NP_001358961.1:p.Ala43Val
NM_001372033.1:c.128C>T NP_001358962.1:p.Ala43Val
NM_001372034.1:c.128C>T NP_001358963.1:p.Ala43Val
NM_001372035.1:c.128C>T NP_001358964.1:p.Ala43Val
NM_001372036.1:c.87C>T NP_001358965.1:p.Arg29=
NM_001372037.1:c.87C>T NP_001358966.1:p.Arg29=
NM_001372038.1:c.128C>T NP_001358967.1:p.Ala43Val
NM_001372039.1:c.128C>T NP_001358968.1:p.Ala43Val
NM_001372040.1:c.128C>T NP_001358969.1:p.Ala43Val
NM_001372041.1:c.128C>T NP_001358970.1:p.Ala43Val
NM_001372042.1:c.-339C>T NP_001358971.1:p.=
NM_001931.5:c.128C>T MANE Select NP_001922.2:p.Ala43Val