Canonical Allele Identifier: CA2615977042

Gene: DLAT

Linked Data

• gnomAD v4: 11-112025352-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112025352T>C , CM000673.2:g.112025352T>C	GRCh38
NC_000011.9:g.111896076T>C , CM000673.1:g.111896076T>C	GRCh37
NC_000011.8:g.111401286T>C	NCBI36
NG_013342.1:g.5539T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713569.1:c.-121T>C	ENSP00000518862.1:n.-121T>C
ENST00000280346.10:c.-121T>C	ENSP00000280346.6:n.-121T>C
NM_001931.4:c.-121T>C	NP_001922.2:n.-121T>C