Canonical Allele Identifier: CA2395758062
Gene: SLC25A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176487T= , CM000684.2:g.19176487T= GRCh38
NC_000022.10:g.19164000T= , CM000684.1:g.19164000T= GRCh37
NC_000022.9:g.17544000T= NCBI36
NG_033863.1:g.7377A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.755A= MANE Select ENSP00000215882.5:p.Glu252=
ENST00000215882.9:c.755A= ENSP00000215882.5:p.Glu252=
ENST00000451283.5:c.446A= ENSP00000401480.1:p.Glu149=
ENST00000470922.5:n.897A=
NM_001256534.1:c.776A= NP_001243463.1:p.Glu259=
NM_001287387.1:c.446A= NP_001274316.1:p.Glu149=
NM_005984.4:c.755A= NP_005975.1:p.Glu252=
NR_046298.2:n.806A=
NM_005984.5:c.755A= MANE Select NP_005975.1:p.Glu252=
NM_001256534.2:c.776A= NP_001243463.1:p.Glu259=
NM_001287387.2:c.446A= NP_001274316.1:p.Glu149=
NR_046298.3:n.679A=