Canonical Allele Identifier: CA2395758074
Gene: SLC25A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176505C= , CM000684.2:g.19176505C= GRCh38
NC_000022.10:g.19164018C= , CM000684.1:g.19164018C= GRCh37
NC_000022.9:g.17544018C= NCBI36
NG_033863.1:g.7359G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.748-11G= MANE Select ENSP00000215882.5:n.748-11G=
ENST00000215882.9:c.748-11G= ENSP00000215882.5:n.748-11G=
ENST00000451283.5:c.439-11G= ENSP00000401480.1:n.439-11G=
ENST00000470922.5:n.890-11G=
NM_001256534.1:c.769-11G= NP_001243463.1:n.769-11G=
NM_001287387.1:c.439-11G= NP_001274316.1:n.439-11G=
NM_005984.4:c.748-11G= NP_005975.1:n.748-11G=
NR_046298.2:n.799-11G=
NM_005984.5:c.748-11G= MANE Select NP_005975.1:n.748-11G=
NM_001256534.2:c.769-11G= NP_001243463.1:n.769-11G=
NM_001287387.2:c.439-11G= NP_001274316.1:n.439-11G=
NR_046298.3:n.672-11G=