Canonical Allele Identifier: CA2000527722

Gene: DLAT

Linked Data

• dbSNP Id: rs1278772770
• gnomAD v4: 11-112025412-C-G

Genomic Alleles

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

Transcript Alleles

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