Canonical Allele Identifier: CA2395758104
Gene: SLC25A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176528G= , CM000684.2:g.19176528G= GRCh38
NC_000022.10:g.19164041G= , CM000684.1:g.19164041G= GRCh37
NC_000022.9:g.17544041G= NCBI36
NG_033863.1:g.7336C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.748-34C= MANE Select ENSP00000215882.5:n.748-34C=
ENST00000215882.9:c.748-34C= ENSP00000215882.5:n.748-34C=
ENST00000451283.5:c.439-34C= ENSP00000401480.1:n.439-34C=
ENST00000470922.5:n.890-34C=
NM_001256534.1:c.769-34C= NP_001243463.1:n.769-34C=
NM_001287387.1:c.439-34C= NP_001274316.1:n.439-34C=
NM_005984.4:c.748-34C= NP_005975.1:n.748-34C=
NR_046298.2:n.799-34C=
NM_005984.5:c.748-34C= MANE Select NP_005975.1:n.748-34C=
NM_001256534.2:c.769-34C= NP_001243463.1:n.769-34C=
NM_001287387.2:c.439-34C= NP_001274316.1:n.439-34C=
NR_046298.3:n.672-34C=