Canonical Allele Identifier: CA2395758232
Gene: SLC25A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176581C= , CM000684.2:g.19176581C= GRCh38
NC_000022.10:g.19164094C= , CM000684.1:g.19164094C= GRCh37
NC_000022.9:g.17544094C= NCBI36
NG_033863.1:g.7283G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.744G= MANE Select ENSP00000215882.5:p.Met248=
ENST00000215882.9:c.744G= ENSP00000215882.5:p.Met248=
ENST00000451283.5:c.435G= ENSP00000401480.1:p.Met145=
ENST00000470922.5:n.886G=
NM_001256534.1:c.765G= NP_001243463.1:p.Met255=
NM_001287387.1:c.435G= NP_001274316.1:p.Met145=
NM_005984.4:c.744G= NP_005975.1:p.Met248=
NR_046298.2:n.795G=
NM_005984.5:c.744G= MANE Select NP_005975.1:p.Met248=
NM_001256534.2:c.765G= NP_001243463.1:p.Met255=
NM_001287387.2:c.435G= NP_001274316.1:p.Met145=
NR_046298.3:n.668G=