Canonical Allele Identifier: CA2395758832
Gene: SLC25A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19177786C= , CM000684.2:g.19177786C= GRCh38
NC_000022.10:g.19165299C= , CM000684.1:g.19165299C= GRCh37
NC_000022.9:g.17545299C= NCBI36
NG_033805.1:g.118931G=
NG_033863.1:g.6078G=

Transcript Alleles

HGVS Amino-acid change
ENST00000215882.10:c.382G= MANE Select ENSP00000215882.5:p.Gly128=
ENST00000215882.9:c.382G= ENSP00000215882.5:p.Gly128=
ENST00000451283.5:c.73G= ENSP00000401480.1:p.Gly25=
ENST00000461267.1:n.528G=
ENST00000470922.5:n.524G=
NM_001256534.1:c.403G= NP_001243463.1:p.Gly135=
NM_001287387.1:c.73G= NP_001274316.1:p.Gly25=
NM_005984.4:c.382G= NP_005975.1:p.Gly128=
NR_046298.2:n.492+156G=
NM_005984.5:c.382G= MANE Select NP_005975.1:p.Gly128=
NM_001256534.2:c.403G= NP_001243463.1:p.Gly135=
NM_001287387.2:c.73G= NP_001274316.1:p.Gly25=
NR_046298.3:n.365+156G=