Canonical Allele Identifier: CA13509828

Gene: DLAT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112044872G>A , CM000673.2:g.112044872G>A	GRCh38
NC_000011.9:g.111915596G>A , CM000673.1:g.111915596G>A	GRCh37
NC_000011.8:g.111420806G>A	NCBI36
NG_013342.1:g.25059G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001931.5:c.1198-266G>A MANE Select	NP_001922.2:n.1198-266G>A
ENST00000280346.11:c.1198-266G>A MANE Select	ENSP00000280346.7:n.1198-266G>A
NM_001372031.1:c.1198-266G>A	NP_001358960.1:n.1198-266G>A
NM_001372032.1:c.1192-266G>A	NP_001358961.1:n.1192-266G>A
NM_001372033.1:c.1198-266G>A	NP_001358962.1:n.1198-266G>A
NM_001372034.1:c.1165-266G>A	NP_001358963.1:n.1165-266G>A
NM_001372035.1:c.1198-266G>A	NP_001358964.1:n.1198-266G>A
NM_001372036.1:c.1072-266G>A	NP_001358965.1:n.1072-266G>A
NM_001372037.1:c.1030-266G>A	NP_001358966.1:n.1030-266G>A
NM_001372038.1:c.919-266G>A	NP_001358967.1:n.919-266G>A
NM_001372039.1:c.883-266G>A	NP_001358968.1:n.883-266G>A
NM_001372040.1:c.817-266G>A	NP_001358969.1:n.817-266G>A
NM_001372041.1:c.883-266G>A	NP_001358970.1:n.883-266G>A
NM_001372042.1:c.736-266G>A	NP_001358971.1:n.736-266G>A
NM_001931.4:c.1198-266G>A	NP_001922.2:n.1198-266G>A
NR_164072.1:n.1075-266G>A
ENST00000280346.10:c.1198-266G>A	ENSP00000280346.6:n.1198-266G>A
ENST00000393051.5:c.883-266G>A	ENSP00000376771.1:n.883-266G>A
ENST00000527231.2:n.1245-266G>A
ENST00000531306.1:c.694-266G>A	ENSP00000433432.1:n.694-266G>A
ENST00000531306.2:c.817-266G>A	ENSP00000433432.2:n.817-266G>A
ENST00000533297.1:c.*873-266G>A	ENSP00000435374.1:n.*873-266G>A
ENST00000679368.1:c.*125-266G>A	ENSP00000505314.1:n.*125-266G>A
ENST00000679466.1:n.1245-266G>A
ENST00000679614.1:c.595-266G>A	ENSP00000506007.1:n.595-266G>A
ENST00000679815.1:c.*631-266G>A	ENSP00000504880.1:n.*631-266G>A
ENST00000679878.1:c.1165-266G>A	ENSP00000505567.1:n.1165-266G>A
ENST00000680010.1:c.*339-266G>A	ENSP00000505768.1:n.*339-266G>A
ENST00000680154.1:n.637-266G>A
ENST00000680331.1:c.919-266G>A	ENSP00000506707.1:n.919-266G>A
ENST00000680411.1:c.943-266G>A	ENSP00000505915.1:n.943-266G>A
ENST00000681316.1:c.1192-266G>A	ENSP00000506560.1:n.1192-266G>A
ENST00000681328.1:c.1198-266G>A	ENSP00000506355.1:n.1198-266G>A
ENST00000681339.1:c.1198-266G>A	ENSP00000506167.1:n.1198-266G>A
ENST00000681638.1:c.*551-266G>A	ENSP00000506090.1:n.*551-266G>A
ENST00000713569.1:c.1198-266G>A	ENSP00000518862.1:n.1198-266G>A
XM_011542647.1:c.1198-266G>A	XP_011540949.1:n.1198-266G>A
XM_011542647.3:c.1198-266G>A	XP_011540949.1:n.1198-266G>A