Canonical Allele Identifier: CA2395757927
Gene: SLC25A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176222G= , CM000684.2:g.19176222G= GRCh38
NC_000022.10:g.19163735G= , CM000684.1:g.19163735G= GRCh37
NC_000022.9:g.17543735G= NCBI36
NG_033863.1:g.7642C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.844C= MANE Select ENSP00000215882.5:p.Arg282=
ENST00000215882.9:c.844C= ENSP00000215882.5:p.Arg282=
ENST00000451283.5:c.535C= ENSP00000401480.1:p.Arg179=
ENST00000470922.5:n.986C=
NM_001256534.1:c.865C= NP_001243463.1:p.Arg289=
NM_001287387.1:c.535C= NP_001274316.1:p.Arg179=
NM_005984.4:c.844C= NP_005975.1:p.Arg282=
NR_046298.2:n.895C=
NM_005984.5:c.844C= MANE Select NP_005975.1:p.Arg282=
NM_001256534.2:c.865C= NP_001243463.1:p.Arg289=
NM_001287387.2:c.535C= NP_001274316.1:p.Arg179=
NR_046298.3:n.768C=