Canonical Allele Identifier: CA2000527735

Gene: DLAT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112025425C= , CM000673.2:g.112025425C=	GRCh38
NC_000011.9:g.111896149C= , CM000673.1:g.111896149C=	GRCh37
NC_000011.8:g.111401359C=	NCBI36
NG_013342.1:g.5612C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713569.1:c.-48C=	ENSP00000518862.1:n.-48C=
ENST00000280346.11:c.-48C= MANE Select	ENSP00000280346.7:n.-48C=
ENST00000679614.1:c.-48C=	ENSP00000506007.1:n.-48C=
ENST00000679815.1:c.-48C=	ENSP00000504880.1:n.-48C=
ENST00000679878.1:c.-48C=	ENSP00000505567.1:n.-48C=
ENST00000280346.10:c.-48C=	ENSP00000280346.6:n.-48C=
ENST00000533297.1:c.-48C=	ENSP00000435374.1:n.-48C=
NM_001931.4:c.-48C=	NP_001922.2:n.-48C=
XM_011542647.1:c.-48C=	XP_011540949.1:n.-48C=
XM_011542647.3:c.-48C=	XP_011540949.1:n.-48C=
NM_001372031.1:c.-48C=	NP_001358960.1:n.-48C=
NM_001372032.1:c.-48C=	NP_001358961.1:n.-48C=
NM_001372033.1:c.-48C=	NP_001358962.1:n.-48C=
NM_001372034.1:c.-48C=	NP_001358963.1:n.-48C=
NM_001372035.1:c.-48C=	NP_001358964.1:n.-48C=
NM_001372036.1:c.-89C=	NP_001358965.1:n.-89C=
NM_001372037.1:c.-89C=	NP_001358966.1:n.-89C=
NM_001372038.1:c.-48C=	NP_001358967.1:n.-48C=
NM_001372039.1:c.-48C=	NP_001358968.1:n.-48C=
NM_001372040.1:c.-48C=	NP_001358969.1:n.-48C=
NM_001372041.1:c.-48C=	NP_001358970.1:n.-48C=
NM_001372042.1:c.-514C=	NP_001358971.1:n.-514C=
NM_001931.5:c.-48C= MANE Select	NP_001922.2:n.-48C=
NR_164072.1:n.18C=