Canonical Allele Identifier: CA6276500
Gene: DLAT HGNC NCBI

Linked Data

ClinVar Variation Id: 377770
ClinVar RCV Id: RCV001705563
dbSNP Id: rs142143586

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112025458G>A , CM000673.2:g.112025458G>A GRCh38
NC_000011.9:g.111896182G>A , CM000673.1:g.111896182G>A GRCh37
NC_000011.8:g.111401392G>A NCBI36
NG_013342.1:g.5645G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000713569.1:c.-15G>A ENSP00000518862.1:n.-15G>A
ENST00000280346.11:c.-15G>A MANE Select ENSP00000280346.7:n.-15G>A
ENST00000527231.2:n.33G>A
ENST00000531306.2:c.-15G>A ENSP00000433432.2:n.-15G>A
ENST00000679368.1:c.-15G>A ENSP00000505314.1:n.-15G>A
ENST00000679466.1:n.33G>A
ENST00000679614.1:c.-15G>A ENSP00000506007.1:n.-15G>A
ENST00000679815.1:c.-15G>A ENSP00000504880.1:n.-15G>A
ENST00000679829.1:n.33G>A
ENST00000679878.1:c.-15G>A ENSP00000505567.1:n.-15G>A
ENST00000680010.1:c.-15G>A ENSP00000505768.1:n.-15G>A
ENST00000680331.1:c.-15G>A ENSP00000506707.1:n.-15G>A
ENST00000681316.1:c.-15G>A ENSP00000506560.1:n.-15G>A
ENST00000681328.1:c.-15G>A ENSP00000506355.1:n.-15G>A
ENST00000681339.1:c.-15G>A ENSP00000506167.1:n.-15G>A
ENST00000681638.1:c.-15G>A ENSP00000506090.1:n.-15G>A
ENST00000280346.10:c.-15G>A ENSP00000280346.6:n.-15G>A
ENST00000393051.5:c.-15G>A ENSP00000376771.1:n.-15G>A
ENST00000533297.1:c.-15G>A ENSP00000435374.1:n.-15G>A
NM_001931.4:c.-15G>A NP_001922.2:n.-15G>A
XM_011542647.1:c.-15G>A XP_011540949.1:n.-15G>A
XM_011542647.3:c.-15G>A XP_011540949.1:n.-15G>A
NM_001372031.1:c.-15G>A NP_001358960.1:n.-15G>A
NM_001372032.1:c.-15G>A NP_001358961.1:n.-15G>A
NM_001372033.1:c.-15G>A NP_001358962.1:n.-15G>A
NM_001372034.1:c.-15G>A NP_001358963.1:n.-15G>A
NM_001372035.1:c.-15G>A NP_001358964.1:n.-15G>A
NM_001372036.1:c.-56G>A NP_001358965.1:n.-56G>A
NM_001372037.1:c.-56G>A NP_001358966.1:n.-56G>A
NM_001372038.1:c.-15G>A NP_001358967.1:n.-15G>A
NM_001372039.1:c.-15G>A NP_001358968.1:n.-15G>A
NM_001372040.1:c.-15G>A NP_001358969.1:n.-15G>A
NM_001372041.1:c.-15G>A NP_001358970.1:n.-15G>A
NM_001372042.1:c.-481G>A NP_001358971.1:n.-481G>A
NM_001931.5:c.-15G>A MANE Select NP_001922.2:n.-15G>A
NR_164072.1:n.51G>A