Canonical Allele Identifier: CA2395757890
Gene: SLC25A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176136C= , CM000684.2:g.19176136C= GRCh38
NC_000022.10:g.19163649C= , CM000684.1:g.19163649C= GRCh37
NC_000022.9:g.17543649C= NCBI36
NG_033863.1:g.7728G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.930G= MANE Select ENSP00000215882.5:p.Thr310=
ENST00000215882.9:c.930G= ENSP00000215882.5:p.Thr310=
ENST00000451283.5:c.621G= ENSP00000401480.1:p.Thr207=
ENST00000470922.5:n.1072G=
NM_001256534.1:c.951G= NP_001243463.1:p.Thr317=
NM_001287387.1:c.621G= NP_001274316.1:p.Thr207=
NM_005984.4:c.930G= NP_005975.1:p.Thr310=
NR_046298.2:n.981G=
NM_005984.5:c.930G= MANE Select NP_005975.1:p.Thr310=
NM_001256534.2:c.951G= NP_001243463.1:p.Thr317=
NM_001287387.2:c.621G= NP_001274316.1:p.Thr207=
NR_046298.3:n.854G=