Canonical Allele Identifier: CA3054209091

Gene: DLAT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112037438_112037439delinsCA , CM000673.2:g.112037438_112037439delinsCA	GRCh38
NC_000011.9:g.111908162_111908163delinsCA , CM000673.1:g.111908162_111908163delinsCA	GRCh37
NC_000011.8:g.111413372_111413373delinsCA	NCBI36
NG_013342.1:g.17625_17626delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713569.1:c.953_954delinsCA	ENSP00000518862.1:p.Val318Ala
ENST00000280346.11:c.953_954delinsCA MANE Select	ENSP00000280346.7:p.Val318Ala
ENST00000527231.2:n.1000_1001delinsCA
ENST00000531306.2:c.572_573delinsCA	ENSP00000433432.2:p.Val191Ala
ENST00000679368.1:c.788-1806_788-1805delinsCA	ENSP00000505314.1:n.788-1806_788-1805delinsCA
ENST00000679466.1:n.1000_1001delinsCA
ENST00000679614.1:c.350_351delinsCA	ENSP00000506007.1:p.Val117Ala
ENST00000679815.1:c.*386_*387delinsCA	ENSP00000504880.1:n.*386_*387delinsCA
ENST00000679829.1:n.1080_1081delinsCA
ENST00000679878.1:c.920_921delinsCA	ENSP00000505567.1:p.Val307Ala
ENST00000680010.1:c.*94_*95delinsCA	ENSP00000505768.1:n.*94_*95delinsCA
ENST00000680331.1:c.674_675delinsCA	ENSP00000506707.1:p.Val225Ala
ENST00000680411.1:c.698_699delinsCA	ENSP00000505915.1:p.Val233Ala
ENST00000681316.1:c.953_954delinsCA	ENSP00000506560.1:p.Val318Ala
ENST00000681328.1:c.953_954delinsCA	ENSP00000506355.1:p.Val318Ala
ENST00000681339.1:c.953_954delinsCA	ENSP00000506167.1:p.Val318Ala
ENST00000681638.1:c.*306_*307delinsCA	ENSP00000506090.1:n.*306_*307delinsCA
ENST00000280346.10:c.953_954delinsCA	ENSP00000280346.6:p.Val318Ala
ENST00000393051.5:c.661-1806_661-1805delinsCA	ENSP00000376771.1:n.661-1806_661-1805delinsCA
ENST00000531306.1:c.449_450delinsCA	ENSP00000433432.1:p.Val150Ala
ENST00000533297.1:c.*628_*629delinsCA	ENSP00000435374.1:n.*628_*629delinsCA
NM_001931.4:c.953_954delinsCA	NP_001922.2:p.Val318Ala
XM_011542647.1:c.953_954delinsCA	XP_011540949.1:p.Val318Ala
XM_011542647.3:c.953_954delinsCA	XP_011540949.1:p.Val318Ala
NM_001372031.1:c.953_954delinsCA	NP_001358960.1:p.Val318Ala
NM_001372032.1:c.953_954delinsCA	NP_001358961.1:p.Val318Ala
NM_001372033.1:c.953_954delinsCA	NP_001358962.1:p.Val318Ala
NM_001372034.1:c.920_921delinsCA	NP_001358963.1:p.Val307Ala
NM_001372035.1:c.953_954delinsCA	NP_001358964.1:p.Val318Ala
NM_001372036.1:c.827_828delinsCA	NP_001358965.1:p.Val276Ala
NM_001372037.1:c.785_786delinsCA	NP_001358966.1:p.Val262Ala
NM_001372038.1:c.674_675delinsCA	NP_001358967.1:p.Val225Ala
NM_001372039.1:c.661-1806_661-1805delinsCA	NP_001358968.1:n.661-1806_661-1805delinsCA
NM_001372040.1:c.572_573delinsCA	NP_001358969.1:p.Val191Ala
NM_001372041.1:c.661-1806_661-1805delinsCA	NP_001358970.1:n.661-1806_661-1805delinsCA
NM_001372042.1:c.491_492delinsCA	NP_001358971.1:p.Val164Ala
NM_001931.5:c.953_954delinsCA MANE Select	NP_001922.2:p.Val318Ala
NR_164072.1:n.853-1806_853-1805delinsCA