Canonical Allele Identifier: CA410636569

Gene: SLC25A1

Linked Data

• MyVariant Identifiers: chr22:g.19164171T>C (hg19) ; chr22:g.19176658T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19176658T>C , CM000684.2:g.19176658T>C	GRCh38
NC_000022.10:g.19164171T>C , CM000684.1:g.19164171T>C	GRCh37
NC_000022.9:g.17544171T>C	NCBI36
NG_033863.1:g.7206A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.667A>G MANE Select	ENSP00000215882.5:p.Thr223Ala
ENST00000215882.9:c.667A>G	ENSP00000215882.5:p.Thr223Ala
ENST00000451283.5:c.358A>G	ENSP00000401480.1:p.Thr120Ala
ENST00000470922.5:n.809A>G
NM_001256534.1:c.688A>G	NP_001243463.1:p.Thr230Ala
NM_001287387.1:c.358A>G	NP_001274316.1:p.Thr120Ala
NM_005984.4:c.667A>G	NP_005975.1:p.Thr223Ala
NR_046298.2:n.718A>G
NM_005984.5:c.667A>G MANE Select	NP_005975.1:p.Thr223Ala
NM_001256534.2:c.688A>G	NP_001243463.1:p.Thr230Ala
NM_001287387.2:c.358A>G	NP_001274316.1:p.Thr120Ala
NR_046298.3:n.591A>G