Canonical Allele Identifier: CA2395758058
Gene: SLC25A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176481T= , CM000684.2:g.19176481T= GRCh38
NC_000022.10:g.19163994T= , CM000684.1:g.19163994T= GRCh37
NC_000022.9:g.17543994T= NCBI36
NG_033863.1:g.7383A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.761A= MANE Select ENSP00000215882.5:p.His254=
ENST00000215882.9:c.761A= ENSP00000215882.5:p.His254=
ENST00000451283.5:c.452A= ENSP00000401480.1:p.His151=
ENST00000470922.5:n.903A=
NM_001256534.1:c.782A= NP_001243463.1:p.His261=
NM_001287387.1:c.452A= NP_001274316.1:p.His151=
NM_005984.4:c.761A= NP_005975.1:p.His254=
NR_046298.2:n.812A=
NM_005984.5:c.761A= MANE Select NP_005975.1:p.His254=
NM_001256534.2:c.782A= NP_001243463.1:p.His261=
NM_001287387.2:c.452A= NP_001274316.1:p.His151=
NR_046298.3:n.685A=