Canonical Allele Identifier: CA2395758574
Gene: SLC25A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19177080C= , CM000684.2:g.19177080C= GRCh38
NC_000022.10:g.19164593C= , CM000684.1:g.19164593C= GRCh37
NC_000022.9:g.17544593C= NCBI36
NG_033863.1:g.6784G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.526+40G= MANE Select ENSP00000215882.5:n.526+40G=
ENST00000215882.9:c.526+40G= ENSP00000215882.5:n.526+40G=
ENST00000451283.5:c.217+40G= ENSP00000401480.1:n.217+40G=
ENST00000461267.1:n.672+40G=
ENST00000470922.5:n.668+40G=
NM_001256534.1:c.547+40G= NP_001243463.1:n.547+40G=
NM_001287387.1:c.217+40G= NP_001274316.1:n.217+40G=
NM_005984.4:c.526+40G= NP_005975.1:n.526+40G=
NR_046298.2:n.577+40G=
NM_005984.5:c.526+40G= MANE Select NP_005975.1:n.526+40G=
NM_001256534.2:c.547+40G= NP_001243463.1:n.547+40G=
NM_001287387.2:c.217+40G= NP_001274316.1:n.217+40G=
NR_046298.3:n.450+40G=