Canonical Allele Identifier: CA410636598
Gene: SLC25A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176661T>G , CM000684.2:g.19176661T>G GRCh38
NC_000022.10:g.19164174T>G , CM000684.1:g.19164174T>G GRCh37
NC_000022.9:g.17544174T>G NCBI36
NG_033863.1:g.7203A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000215882.10:c.664A>C MANE Select ENSP00000215882.5:p.Ile222Leu
ENST00000215882.9:c.664A>C ENSP00000215882.5:p.Ile222Leu
ENST00000451283.5:c.355A>C ENSP00000401480.1:p.Ile119Leu
ENST00000470922.5:n.806A>C
NM_001256534.1:c.685A>C NP_001243463.1:p.Ile229Leu
NM_001287387.1:c.355A>C NP_001274316.1:p.Ile119Leu
NM_005984.4:c.664A>C NP_005975.1:p.Ile222Leu
NR_046298.2:n.715A>C
NM_005984.5:c.664A>C MANE Select NP_005975.1:p.Ile222Leu
NM_001256534.2:c.685A>C NP_001243463.1:p.Ile229Leu
NM_001287387.2:c.355A>C NP_001274316.1:p.Ile119Leu
NR_046298.3:n.588A>C