Canonical Allele Identifier: CA2395758717
Gene: SLC25A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19177601C= , CM000684.2:g.19177601C= GRCh38
NC_000022.10:g.19165114C= , CM000684.1:g.19165114C= GRCh37
NC_000022.9:g.17545114C= NCBI36
NG_033805.1:g.119116G=
NG_033863.1:g.6263G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.441+126G= MANE Select ENSP00000215882.5:n.441+126G=
ENST00000215882.9:c.441+126G= ENSP00000215882.5:n.441+126G=
ENST00000451283.5:c.132+126G= ENSP00000401480.1:n.132+126G=
ENST00000461267.1:n.587+126G=
ENST00000470922.5:n.583+126G=
NM_001256534.1:c.462+126G= NP_001243463.1:n.462+126G=
NM_001287387.1:c.132+126G= NP_001274316.1:n.132+126G=
NM_005984.4:c.441+126G= NP_005975.1:n.441+126G=
NR_046298.2:n.492+341G=
NM_005984.5:c.441+126G= MANE Select NP_005975.1:n.441+126G=
NM_001256534.2:c.462+126G= NP_001243463.1:n.462+126G=
NM_001287387.2:c.132+126G= NP_001274316.1:n.132+126G=
NR_046298.3:n.365+341G=