Canonical Allele Identifier: CA6276880

Gene: DLAT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112045279del , CM000673.2:g.112045279del	GRCh38
NC_000011.9:g.111916003del , CM000673.1:g.111916003del	GRCh37
NC_000011.8:g.111421213del	NCBI36
NG_013342.1:g.25466del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713569.1:c.1290+49del	ENSP00000518862.1:n.1290+49del
ENST00000280346.11:c.1290+49del MANE Select	ENSP00000280346.7:n.1290+49del
ENST00000527231.2:n.1337+49del
ENST00000531306.2:c.909+49del	ENSP00000433432.2:n.909+49del
ENST00000679368.1:c.*217+49del	ENSP00000505314.1:n.*217+49del
ENST00000679466.1:n.1337+49del
ENST00000679614.1:c.687+49del	ENSP00000506007.1:n.687+49del
ENST00000679815.1:c.*723+49del	ENSP00000504880.1:n.*723+49del
ENST00000679878.1:c.1257+49del	ENSP00000505567.1:n.1257+49del
ENST00000680010.1:c.*431+49del	ENSP00000505768.1:n.*431+49del
ENST00000680154.1:n.729+49del
ENST00000680331.1:c.1011+49del	ENSP00000506707.1:n.1011+49del
ENST00000680411.1:c.1035+49del	ENSP00000505915.1:n.1035+49del
ENST00000681316.1:c.1284+49del	ENSP00000506560.1:n.1284+49del
ENST00000681328.1:c.1290+49del	ENSP00000506355.1:n.1290+49del
ENST00000681339.1:c.1290+49del	ENSP00000506167.1:n.1290+49del
ENST00000681638.1:c.*643+49del	ENSP00000506090.1:n.*643+49del
ENST00000280346.10:c.1290+49del	ENSP00000280346.6:n.1290+49del
ENST00000393051.5:c.975+49del	ENSP00000376771.1:n.975+49del
ENST00000531306.1:c.786+49del	ENSP00000433432.1:n.786+49del
ENST00000533297.1:c.*965+49del	ENSP00000435374.1:n.*965+49del
NM_001931.4:c.1290+49del	NP_001922.2:n.1290+49del
XM_011542647.1:c.1290+49del	XP_011540949.1:n.1290+49del
XM_011542647.3:c.1290+49del	XP_011540949.1:n.1290+49del
NM_001372031.1:c.1290+49del	NP_001358960.1:n.1290+49del
NM_001372032.1:c.1284+49del	NP_001358961.1:n.1284+49del
NM_001372033.1:c.1290+49del	NP_001358962.1:n.1290+49del
NM_001372034.1:c.1257+49del	NP_001358963.1:n.1257+49del
NM_001372035.1:c.1290+49del	NP_001358964.1:n.1290+49del
NM_001372036.1:c.1164+49del	NP_001358965.1:n.1164+49del
NM_001372037.1:c.1122+49del	NP_001358966.1:n.1122+49del
NM_001372038.1:c.1011+49del	NP_001358967.1:n.1011+49del
NM_001372039.1:c.975+49del	NP_001358968.1:n.975+49del
NM_001372040.1:c.909+49del	NP_001358969.1:n.909+49del
NM_001372041.1:c.975+49del	NP_001358970.1:n.975+49del
NM_001372042.1:c.828+49del	NP_001358971.1:n.828+49del
NM_001931.5:c.1290+49del MANE Select	NP_001922.2:n.1290+49del
NR_164072.1:n.1167+49del