Canonical Allele Identifier: CA382600666

Gene: DLAT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112028615C>T , CM000673.2:g.112028615C>T	GRCh38
NC_000011.9:g.111899339C>T , CM000673.1:g.111899339C>T	GRCh37
NC_000011.8:g.111404549C>T	NCBI36
NG_013342.1:g.8802C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001931.5:c.482C>T MANE Select	NP_001922.2:p.Ala161Val
ENST00000280346.11:c.482C>T MANE Select	ENSP00000280346.7:p.Ala161Val
NM_001372031.1:c.482C>T	NP_001358960.1:p.Ala161Val
NM_001372032.1:c.482C>T	NP_001358961.1:p.Ala161Val
NM_001372033.1:c.482C>T	NP_001358962.1:p.Ala161Val
NM_001372034.1:c.449C>T	NP_001358963.1:p.Ala150Val
NM_001372035.1:c.482C>T	NP_001358964.1:p.Ala161Val
NM_001372036.1:c.356C>T	NP_001358965.1:p.Ala119Val
NM_001372037.1:c.314C>T	NP_001358966.1:p.Ala105Val
NM_001372038.1:c.381+2316C>T	NP_001358967.1:n.381+2316C>T
NM_001372039.1:c.482C>T	NP_001358968.1:p.Ala161Val
NM_001372040.1:c.364+2333C>T	NP_001358969.1:n.364+2333C>T
NM_001372041.1:c.482C>T	NP_001358970.1:p.Ala161Val
NM_001372042.1:c.16C>T	NP_001358971.1:p.Arg6Ter
NM_001931.4:c.482C>T	NP_001922.2:p.Ala161Val
NR_164072.1:n.547C>T
ENST00000280346.10:c.482C>T	ENSP00000280346.6:p.Ala161Val
ENST00000393051.5:c.482C>T	ENSP00000376771.1:p.Ala161Val
ENST00000527231.2:n.529C>T
ENST00000531306.1:c.241+2333C>T	ENSP00000433432.1:n.241+2333C>T
ENST00000531306.2:c.364+2333C>T	ENSP00000433432.2:n.364+2333C>T
ENST00000533297.1:c.*157C>T	ENSP00000435374.1:n.*157C>T
ENST00000679368.1:c.482C>T	ENSP00000505314.1:p.Ala161Val
ENST00000679466.1:n.529C>T
ENST00000679614.1:c.25-298C>T	ENSP00000506007.1:n.25-298C>T
ENST00000679815.1:c.482C>T	ENSP00000504880.1:p.Ala161Val
ENST00000679829.1:n.529C>T
ENST00000679878.1:c.449C>T	ENSP00000505567.1:p.Ala150Val
ENST00000680010.1:c.482C>T	ENSP00000505768.1:p.Ala161Val
ENST00000680331.1:c.381+2316C>T	ENSP00000506707.1:n.381+2316C>T
ENST00000680411.1:c.227C>T	ENSP00000505915.1:p.Ala76Val
ENST00000681316.1:c.482C>T	ENSP00000506560.1:p.Ala161Val
ENST00000681328.1:c.482C>T	ENSP00000506355.1:p.Ala161Val
ENST00000681339.1:c.482C>T	ENSP00000506167.1:p.Ala161Val
ENST00000681638.1:c.482C>T	ENSP00000506090.1:p.Ala161Val
ENST00000713569.1:c.482C>T	ENSP00000518862.1:p.Ala161Val
XM_011542647.1:c.482C>T	XP_011540949.1:p.Ala161Val
XM_011542647.3:c.482C>T	XP_011540949.1:p.Ala161Val