Canonical Allele Identifier: CA2395757904
Gene: SLC25A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176168C= , CM000684.2:g.19176168C= GRCh38
NC_000022.10:g.19163681C= , CM000684.1:g.19163681C= GRCh37
NC_000022.9:g.17543681C= NCBI36
NG_033863.1:g.7696G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.898G= MANE Select ENSP00000215882.5:p.Val300=
ENST00000215882.9:c.898G= ENSP00000215882.5:p.Val300=
ENST00000451283.5:c.589G= ENSP00000401480.1:p.Val197=
ENST00000470922.5:n.1040G=
NM_001256534.1:c.919G= NP_001243463.1:p.Val307=
NM_001287387.1:c.589G= NP_001274316.1:p.Val197=
NM_005984.4:c.898G= NP_005975.1:p.Val300=
NR_046298.2:n.949G=
NM_005984.5:c.898G= MANE Select NP_005975.1:p.Val300=
NM_001256534.2:c.919G= NP_001243463.1:p.Val307=
NM_001287387.2:c.589G= NP_001274316.1:p.Val197=
NR_046298.3:n.822G=