Canonical Allele Identifier: CA2615977099

Gene: DLAT

Linked Data

• gnomAD v4: 11-112025412-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112025412C>A , CM000673.2:g.112025412C>A	GRCh38
NC_000011.9:g.111896136C>A , CM000673.1:g.111896136C>A	GRCh37
NC_000011.8:g.111401346C>A	NCBI36
NG_013342.1:g.5599C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713569.1:c.-61C>A	ENSP00000518862.1:n.-61C>A
ENST00000280346.11:c.-61C>A MANE Select	ENSP00000280346.7:n.-61C>A
ENST00000679614.1:c.-61C>A	ENSP00000506007.1:n.-61C>A
ENST00000679815.1:c.-61C>A	ENSP00000504880.1:n.-61C>A
ENST00000679878.1:c.-61C>A	ENSP00000505567.1:n.-61C>A
ENST00000280346.10:c.-61C>A	ENSP00000280346.6:n.-61C>A
ENST00000533297.1:c.-61C>A	ENSP00000435374.1:n.-61C>A
NM_001931.4:c.-61C>A	NP_001922.2:n.-61C>A
XM_011542647.1:c.-61C>A	XP_011540949.1:n.-61C>A
XM_011542647.3:c.-61C>A	XP_011540949.1:n.-61C>A
NM_001372031.1:c.-61C>A	NP_001358960.1:n.-61C>A
NM_001372032.1:c.-61C>A	NP_001358961.1:n.-61C>A
NM_001372033.1:c.-61C>A	NP_001358962.1:n.-61C>A
NM_001372034.1:c.-61C>A	NP_001358963.1:n.-61C>A
NM_001372035.1:c.-61C>A	NP_001358964.1:n.-61C>A
NM_001372036.1:c.-102C>A	NP_001358965.1:n.-102C>A
NM_001372037.1:c.-102C>A	NP_001358966.1:n.-102C>A
NM_001372038.1:c.-61C>A	NP_001358967.1:n.-61C>A
NM_001372039.1:c.-61C>A	NP_001358968.1:n.-61C>A
NM_001372040.1:c.-61C>A	NP_001358969.1:n.-61C>A
NM_001372041.1:c.-61C>A	NP_001358970.1:n.-61C>A
NM_001372042.1:c.-527C>A	NP_001358971.1:n.-527C>A
NM_001931.5:c.-61C>A MANE Select	NP_001922.2:n.-61C>A
NR_164072.1:n.5C>A