Canonical Allele Identifier: CA2395758558
Gene: SLC25A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19177048G= , CM000684.2:g.19177048G= GRCh38
NC_000022.10:g.19164561G= , CM000684.1:g.19164561G= GRCh37
NC_000022.9:g.17544561G= NCBI36
NG_033863.1:g.6816C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.526+72C= MANE Select ENSP00000215882.5:n.526+72C=
ENST00000215882.9:c.526+72C= ENSP00000215882.5:n.526+72C=
ENST00000451283.5:c.217+72C= ENSP00000401480.1:n.217+72C=
ENST00000461267.1:n.672+72C=
ENST00000470922.5:n.668+72C=
NM_001256534.1:c.547+72C= NP_001243463.1:n.547+72C=
NM_001287387.1:c.217+72C= NP_001274316.1:n.217+72C=
NM_005984.4:c.526+72C= NP_005975.1:n.526+72C=
NR_046298.2:n.577+72C=
NM_005984.5:c.526+72C= MANE Select NP_005975.1:n.526+72C=
NM_001256534.2:c.547+72C= NP_001243463.1:n.547+72C=
NM_001287387.2:c.217+72C= NP_001274316.1:n.217+72C=
NR_046298.3:n.450+72C=