Canonical Allele Identifier: CA2395758467
Gene: SLC25A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176911A= , CM000684.2:g.19176911A= GRCh38
NC_000022.10:g.19164424A= , CM000684.1:g.19164424A= GRCh37
NC_000022.9:g.17544424A= NCBI36
NG_033863.1:g.6953T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.566T= MANE Select ENSP00000215882.5:p.Leu189=
ENST00000215882.9:c.566T= ENSP00000215882.5:p.Leu189=
ENST00000451283.5:c.257T= ENSP00000401480.1:p.Leu86=
ENST00000461267.1:n.712T=
ENST00000470922.5:n.708T=
NM_001256534.1:c.587T= NP_001243463.1:p.Leu196=
NM_001287387.1:c.257T= NP_001274316.1:p.Leu86=
NM_005984.4:c.566T= NP_005975.1:p.Leu189=
NR_046298.2:n.617T=
NM_005984.5:c.566T= MANE Select NP_005975.1:p.Leu189=
NM_001256534.2:c.587T= NP_001243463.1:p.Leu196=
NM_001287387.2:c.257T= NP_001274316.1:p.Leu86=
NR_046298.3:n.490T=