Canonical Allele Identifier: CA2395757898
Gene: SLC25A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176156G= , CM000684.2:g.19176156G= GRCh38
NC_000022.10:g.19163669G= , CM000684.1:g.19163669G= GRCh37
NC_000022.9:g.17543669G= NCBI36
NG_033863.1:g.7708C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.910C= MANE Select ENSP00000215882.5:p.Leu304=
ENST00000215882.9:c.910C= ENSP00000215882.5:p.Leu304=
ENST00000451283.5:c.601C= ENSP00000401480.1:p.Leu201=
ENST00000470922.5:n.1052C=
NM_001256534.1:c.931C= NP_001243463.1:p.Leu311=
NM_001287387.1:c.601C= NP_001274316.1:p.Leu201=
NM_005984.4:c.910C= NP_005975.1:p.Leu304=
NR_046298.2:n.961C=
NM_005984.5:c.910C= MANE Select NP_005975.1:p.Leu304=
NM_001256534.2:c.931C= NP_001243463.1:p.Leu311=
NM_001287387.2:c.601C= NP_001274316.1:p.Leu201=
NR_046298.3:n.834C=