Canonical Allele Identifier: CA2395758339
Gene: SLC25A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176691C= , CM000684.2:g.19176691C= GRCh38
NC_000022.10:g.19164204C= , CM000684.1:g.19164204C= GRCh37
NC_000022.9:g.17544204C= NCBI36
NG_033863.1:g.7173G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.634G= MANE Select ENSP00000215882.5:p.Asp212=
ENST00000215882.9:c.634G= ENSP00000215882.5:p.Asp212=
ENST00000451283.5:c.325G= ENSP00000401480.1:p.Asp109=
ENST00000461267.1:n.780G=
ENST00000470922.5:n.776G=
NM_001256534.1:c.655G= NP_001243463.1:p.Asp219=
NM_001287387.1:c.325G= NP_001274316.1:p.Asp109=
NM_005984.4:c.634G= NP_005975.1:p.Asp212=
NR_046298.2:n.685G=
NM_005984.5:c.634G= MANE Select NP_005975.1:p.Asp212=
NM_001256534.2:c.655G= NP_001243463.1:p.Asp219=
NM_001287387.2:c.325G= NP_001274316.1:p.Asp109=
NR_046298.3:n.558G=