Canonical Allele Identifier: CA2000527741

Gene: DLAT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112025432G= , CM000673.2:g.112025432G=	GRCh38
NC_000011.9:g.111896156G= , CM000673.1:g.111896156G=	GRCh37
NC_000011.8:g.111401366G=	NCBI36
NG_013342.1:g.5619G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713569.1:c.-41G=	ENSP00000518862.1:n.-41G=
ENST00000280346.11:c.-41G= MANE Select	ENSP00000280346.7:n.-41G=
ENST00000527231.2:n.7G=
ENST00000531306.2:c.-41G=	ENSP00000433432.2:n.-41G=
ENST00000679368.1:c.-41G=	ENSP00000505314.1:n.-41G=
ENST00000679466.1:n.7G=
ENST00000679614.1:c.-41G=	ENSP00000506007.1:n.-41G=
ENST00000679815.1:c.-41G=	ENSP00000504880.1:n.-41G=
ENST00000679829.1:n.7G=
ENST00000679878.1:c.-41G=	ENSP00000505567.1:n.-41G=
ENST00000680010.1:c.-41G=	ENSP00000505768.1:n.-41G=
ENST00000681316.1:c.-41G=	ENSP00000506560.1:n.-41G=
ENST00000681328.1:c.-41G=	ENSP00000506355.1:n.-41G=
ENST00000681339.1:c.-41G=	ENSP00000506167.1:n.-41G=
ENST00000681638.1:c.-41G=	ENSP00000506090.1:n.-41G=
ENST00000280346.10:c.-41G=	ENSP00000280346.6:n.-41G=
ENST00000533297.1:c.-41G=	ENSP00000435374.1:n.-41G=
NM_001931.4:c.-41G=	NP_001922.2:n.-41G=
XM_011542647.1:c.-41G=	XP_011540949.1:n.-41G=
XM_011542647.3:c.-41G=	XP_011540949.1:n.-41G=
NM_001372031.1:c.-41G=	NP_001358960.1:n.-41G=
NM_001372032.1:c.-41G=	NP_001358961.1:n.-41G=
NM_001372033.1:c.-41G=	NP_001358962.1:n.-41G=
NM_001372034.1:c.-41G=	NP_001358963.1:n.-41G=
NM_001372035.1:c.-41G=	NP_001358964.1:n.-41G=
NM_001372036.1:c.-82G=	NP_001358965.1:n.-82G=
NM_001372037.1:c.-82G=	NP_001358966.1:n.-82G=
NM_001372038.1:c.-41G=	NP_001358967.1:n.-41G=
NM_001372039.1:c.-41G=	NP_001358968.1:n.-41G=
NM_001372040.1:c.-41G=	NP_001358969.1:n.-41G=
NM_001372041.1:c.-41G=	NP_001358970.1:n.-41G=
NM_001372042.1:c.-507G=	NP_001358971.1:n.-507G=
NM_001931.5:c.-41G= MANE Select	NP_001922.2:n.-41G=
NR_164072.1:n.25G=