Canonical Allele Identifier: CA10637613

Gene: DLAT

Linked Data

• ClinVar Variation Id: 302447
• ClinVar RCV Id: RCV001552510
• dbSNP Id: rs115067052
• gnomAD v2: 11-111896041-C-G
• gnomAD v3: 11-112025317-C-G
• gnomAD v4: 11-112025317-C-G
• MyVariant Identifiers: chr11:g.111896041C>G (hg19) ; chr11:g.112025317C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112025317C>G , CM000673.2:g.112025317C>G	GRCh38
NC_000011.9:g.111896041C>G , CM000673.1:g.111896041C>G	GRCh37
NC_000011.8:g.111401251C>G	NCBI36
NG_013342.1:g.5504C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713569.1:c.-156C>G	ENSP00000518862.1:n.-156C>G
ENST00000280346.10:c.-156C>G	ENSP00000280346.6:n.-156C>G
NM_001931.4:c.-156C>G	NP_001922.2:n.-156C>G