Canonical Allele Identifier: CA2000527906
Gene: DLAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112025723G= , CM000673.2:g.112025723G= GRCh38
NC_000011.9:g.111896447G= , CM000673.1:g.111896447G= GRCh37
NC_000011.8:g.111401657G= NCBI36
NG_013342.1:g.5910G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000713569.1:c.251G= ENSP00000518862.1:p.Arg84=
ENST00000280346.11:c.251G= MANE Select ENSP00000280346.7:p.Arg84=
ENST00000527231.2:n.298G=
ENST00000531306.2:c.251G= ENSP00000433432.2:p.Arg84=
ENST00000679368.1:c.251G= ENSP00000505314.1:p.Arg84=
ENST00000679466.1:n.298G=
ENST00000679614.1:c.24+227G= ENSP00000506007.1:n.24+227G=
ENST00000679815.1:c.251G= ENSP00000504880.1:p.Arg84=
ENST00000679829.1:n.298G=
ENST00000679878.1:c.251G= ENSP00000505567.1:p.Arg84=
ENST00000680010.1:c.251G= ENSP00000505768.1:p.Arg84=
ENST00000680331.1:c.251G= ENSP00000506707.1:p.Arg84=
ENST00000681316.1:c.251G= ENSP00000506560.1:p.Arg84=
ENST00000681328.1:c.251G= ENSP00000506355.1:p.Arg84=
ENST00000681339.1:c.251G= ENSP00000506167.1:p.Arg84=
ENST00000681638.1:c.251G= ENSP00000506090.1:p.Arg84=
ENST00000280346.10:c.251G= ENSP00000280346.6:p.Arg84=
ENST00000393051.5:c.251G= ENSP00000376771.1:p.Arg84=
ENST00000531306.1:c.128G= ENSP00000433432.1:p.Arg43=
ENST00000533297.1:c.152+99G= ENSP00000435374.1:n.152+99G=
NM_001931.4:c.251G= NP_001922.2:p.Arg84=
XM_011542647.1:c.251G= XP_011540949.1:p.Arg84=
XM_011542647.3:c.251G= XP_011540949.1:p.Arg84=
NM_001372031.1:c.251G= NP_001358960.1:p.Arg84=
NM_001372032.1:c.251G= NP_001358961.1:p.Arg84=
NM_001372033.1:c.251G= NP_001358962.1:p.Arg84=
NM_001372034.1:c.251G= NP_001358963.1:p.Arg84=
NM_001372035.1:c.251G= NP_001358964.1:p.Arg84=
NM_001372036.1:c.210G= NP_001358965.1:p.Pro70=
NM_001372037.1:c.111+99G= NP_001358966.1:n.111+99G=
NM_001372038.1:c.251G= NP_001358967.1:p.Arg84=
NM_001372039.1:c.251G= NP_001358968.1:p.Arg84=
NM_001372040.1:c.251G= NP_001358969.1:p.Arg84=
NM_001372041.1:c.251G= NP_001358970.1:p.Arg84=
NM_001372042.1:c.-216G= NP_001358971.1:n.-216G=
NM_001931.5:c.251G= MANE Select NP_001922.2:p.Arg84=
NR_164072.1:n.316G=