Canonical Allele Identifier: CA476790731

Gene: DLAT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112039339T>C , CM000673.2:g.112039339T>C	GRCh38
NC_000011.9:g.111910063T>C , CM000673.1:g.111910063T>C	GRCh37
NC_000011.8:g.111415273T>C	NCBI36
NG_013342.1:g.19526T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713569.1:c.1071T>C	ENSP00000518862.1:p.Val357=
ENST00000280346.11:c.1071T>C MANE Select	ENSP00000280346.7:p.Val357=
ENST00000527231.2:n.1118T>C
ENST00000531306.2:c.690T>C	ENSP00000433432.2:p.Val230=
ENST00000679368.1:c.883T>C	ENSP00000505314.1:p.Ter295Gln
ENST00000679466.1:n.1118T>C
ENST00000679614.1:c.468T>C	ENSP00000506007.1:p.Val156=
ENST00000679815.1:c.*504T>C	ENSP00000504880.1:n.*504T>C
ENST00000679829.1:n.1198T>C
ENST00000679878.1:c.1038T>C	ENSP00000505567.1:p.Val346=
ENST00000680010.1:c.*212T>C	ENSP00000505768.1:n.*212T>C
ENST00000680331.1:c.792T>C	ENSP00000506707.1:p.Val264=
ENST00000680411.1:c.816T>C	ENSP00000505915.1:p.Val272=
ENST00000681316.1:c.1071T>C	ENSP00000506560.1:p.Val357=
ENST00000681328.1:c.1071T>C	ENSP00000506355.1:p.Val357=
ENST00000681339.1:c.1071T>C	ENSP00000506167.1:p.Val357=
ENST00000681638.1:c.*424T>C	ENSP00000506090.1:n.*424T>C
ENST00000280346.10:c.1071T>C	ENSP00000280346.6:p.Val357=
ENST00000393051.5:c.756T>C	ENSP00000376771.1:p.Val252=
ENST00000531306.1:c.567T>C	ENSP00000433432.1:p.Val189=
ENST00000533297.1:c.*746T>C	ENSP00000435374.1:n.*746T>C
NM_001931.4:c.1071T>C	NP_001922.2:p.Val357=
XM_011542647.1:c.1071T>C	XP_011540949.1:p.Val357=
XM_011542647.3:c.1071T>C	XP_011540949.1:p.Val357=
NM_001372031.1:c.1071T>C	NP_001358960.1:p.Val357=
NM_001372032.1:c.1071T>C	NP_001358961.1:p.Val357=
NM_001372033.1:c.1071T>C	NP_001358962.1:p.Val357=
NM_001372034.1:c.1038T>C	NP_001358963.1:p.Val346=
NM_001372035.1:c.1071T>C	NP_001358964.1:p.Val357=
NM_001372036.1:c.945T>C	NP_001358965.1:p.Val315=
NM_001372037.1:c.903T>C	NP_001358966.1:p.Val301=
NM_001372038.1:c.792T>C	NP_001358967.1:p.Val264=
NM_001372039.1:c.756T>C	NP_001358968.1:p.Val252=
NM_001372040.1:c.690T>C	NP_001358969.1:p.Val230=
NM_001372041.1:c.756T>C	NP_001358970.1:p.Val252=
NM_001372042.1:c.609T>C	NP_001358971.1:p.Val203=
NM_001931.5:c.1071T>C MANE Select	NP_001922.2:p.Val357=
NR_164072.1:n.948T>C