Canonical Allele Identifier: CA2395758328
Gene: SLC25A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176671C= , CM000684.2:g.19176671C= GRCh38
NC_000022.10:g.19164184C= , CM000684.1:g.19164184C= GRCh37
NC_000022.9:g.17544184C= NCBI36
NG_033863.1:g.7193G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.654G= MANE Select ENSP00000215882.5:p.Met218=
ENST00000215882.9:c.654G= ENSP00000215882.5:p.Met218=
ENST00000451283.5:c.345G= ENSP00000401480.1:p.Met115=
ENST00000461267.1:n.800G=
ENST00000470922.5:n.796G=
NM_001256534.1:c.675G= NP_001243463.1:p.Met225=
NM_001287387.1:c.345G= NP_001274316.1:p.Met115=
NM_005984.4:c.654G= NP_005975.1:p.Met218=
NR_046298.2:n.705G=
NM_005984.5:c.654G= MANE Select NP_005975.1:p.Met218=
NM_001256534.2:c.675G= NP_001243463.1:p.Met225=
NM_001287387.2:c.345G= NP_001274316.1:p.Met115=
NR_046298.3:n.578G=