Canonical Allele Identifier: CA2395758257
Gene: SLC25A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176589T= , CM000684.2:g.19176589T= GRCh38
NC_000022.10:g.19164102T= , CM000684.1:g.19164102T= GRCh37
NC_000022.9:g.17544102T= NCBI36
NG_033863.1:g.7275A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.736A= MANE Select ENSP00000215882.5:p.Thr246=
ENST00000215882.9:c.736A= ENSP00000215882.5:p.Thr246=
ENST00000451283.5:c.427A= ENSP00000401480.1:p.Thr143=
ENST00000470922.5:n.878A=
NM_001256534.1:c.757A= NP_001243463.1:p.Thr253=
NM_001287387.1:c.427A= NP_001274316.1:p.Thr143=
NM_005984.4:c.736A= NP_005975.1:p.Thr246=
NR_046298.2:n.787A=
NM_005984.5:c.736A= MANE Select NP_005975.1:p.Thr246=
NM_001256534.2:c.757A= NP_001243463.1:p.Thr253=
NM_001287387.2:c.427A= NP_001274316.1:p.Thr143=
NR_046298.3:n.660A=