Canonical Allele Identifier: CA2395757932
Gene: SLC25A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176232G= , CM000684.2:g.19176232G= GRCh38
NC_000022.10:g.19163745G= , CM000684.1:g.19163745G= GRCh37
NC_000022.9:g.17543745G= NCBI36
NG_033863.1:g.7632C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.834C= MANE Select ENSP00000215882.5:p.Gly278=
ENST00000215882.9:c.834C= ENSP00000215882.5:p.Gly278=
ENST00000451283.5:c.525C= ENSP00000401480.1:p.Gly175=
ENST00000470922.5:n.976C=
NM_001256534.1:c.855C= NP_001243463.1:p.Gly285=
NM_001287387.1:c.525C= NP_001274316.1:p.Gly175=
NM_005984.4:c.834C= NP_005975.1:p.Gly278=
NR_046298.2:n.885C=
NM_005984.5:c.834C= MANE Select NP_005975.1:p.Gly278=
NM_001256534.2:c.855C= NP_001243463.1:p.Gly285=
NM_001287387.2:c.525C= NP_001274316.1:p.Gly175=
NR_046298.3:n.758C=