Canonical Allele Identifier: CA382596528
Gene: DLAT HGNC NCBI

Linked Data

ClinVar Variation Id: 1977862
ClinVar RCV Id: RCV002736836
dbSNP Id: rs782202863

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112025725T>G , CM000673.2:g.112025725T>G GRCh38
NC_000011.9:g.111896449T>G , CM000673.1:g.111896449T>G GRCh37
NC_000011.8:g.111401659T>G NCBI36
NG_013342.1:g.5912T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000713569.1:c.253T>G ENSP00000518862.1:p.Tyr85Asp
ENST00000280346.11:c.253T>G MANE Select ENSP00000280346.7:p.Tyr85Asp
ENST00000527231.2:n.300T>G
ENST00000531306.2:c.253T>G ENSP00000433432.2:p.Tyr85Asp
ENST00000679368.1:c.253T>G ENSP00000505314.1:p.Tyr85Asp
ENST00000679466.1:n.300T>G
ENST00000679614.1:c.24+229T>G ENSP00000506007.1:n.24+229T>G
ENST00000679815.1:c.253T>G ENSP00000504880.1:p.Tyr85Asp
ENST00000679829.1:n.300T>G
ENST00000679878.1:c.253T>G ENSP00000505567.1:p.Tyr85Asp
ENST00000680010.1:c.253T>G ENSP00000505768.1:p.Tyr85Asp
ENST00000680331.1:c.253T>G ENSP00000506707.1:p.Tyr85Asp
ENST00000681316.1:c.253T>G ENSP00000506560.1:p.Tyr85Asp
ENST00000681328.1:c.253T>G ENSP00000506355.1:p.Tyr85Asp
ENST00000681339.1:c.253T>G ENSP00000506167.1:p.Tyr85Asp
ENST00000681638.1:c.253T>G ENSP00000506090.1:p.Tyr85Asp
ENST00000280346.10:c.253T>G ENSP00000280346.6:p.Tyr85Asp
ENST00000393051.5:c.253T>G ENSP00000376771.1:p.Tyr85Asp
ENST00000531306.1:c.130T>G ENSP00000433432.1:p.Tyr44Asp
ENST00000533297.1:c.152+101T>G ENSP00000435374.1:n.152+101T>G
NM_001931.4:c.253T>G NP_001922.2:p.Tyr85Asp
XM_011542647.1:c.253T>G XP_011540949.1:p.Tyr85Asp
XM_011542647.3:c.253T>G XP_011540949.1:p.Tyr85Asp
NM_001372031.1:c.253T>G NP_001358960.1:p.Tyr85Asp
NM_001372032.1:c.253T>G NP_001358961.1:p.Tyr85Asp
NM_001372033.1:c.253T>G NP_001358962.1:p.Tyr85Asp
NM_001372034.1:c.253T>G NP_001358963.1:p.Tyr85Asp
NM_001372035.1:c.253T>G NP_001358964.1:p.Tyr85Asp
NM_001372036.1:c.212T>G NP_001358965.1:p.Leu71Arg
NM_001372037.1:c.111+101T>G NP_001358966.1:n.111+101T>G
NM_001372038.1:c.253T>G NP_001358967.1:p.Tyr85Asp
NM_001372039.1:c.253T>G NP_001358968.1:p.Tyr85Asp
NM_001372040.1:c.253T>G NP_001358969.1:p.Tyr85Asp
NM_001372041.1:c.253T>G NP_001358970.1:p.Tyr85Asp
NM_001372042.1:c.-214T>G NP_001358971.1:n.-214T>G
NM_001931.5:c.253T>G MANE Select NP_001922.2:p.Tyr85Asp
NR_164072.1:n.318T>G