Canonical Allele Identifier: CA410636597
Gene: SLC25A1 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000215882.10:c.664A>G MANE Select ENSP00000215882.5:p.Ile222Val
ENST00000215882.9:c.664A>G ENSP00000215882.5:p.Ile222Val
ENST00000451283.5:c.355A>G ENSP00000401480.1:p.Ile119Val
ENST00000470922.5:n.806A>G
NM_001256534.1:c.685A>G NP_001243463.1:p.Ile229Val
NM_001287387.1:c.355A>G NP_001274316.1:p.Ile119Val
NM_005984.4:c.664A>G NP_005975.1:p.Ile222Val
NR_046298.2:n.715A>G
NM_005984.5:c.664A>G MANE Select NP_005975.1:p.Ile222Val
NM_001256534.2:c.685A>G NP_001243463.1:p.Ile229Val
NM_001287387.2:c.355A>G NP_001274316.1:p.Ile119Val
NR_046298.3:n.588A>G