Canonical Allele Identifier: CA410633761

Gene: SLC25A1

Linked Data

• MyVariant Identifiers: chr22:g.19163698A>C (hg19) ; chr22:g.19176185A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19176185A>C , CM000684.2:g.19176185A>C	GRCh38
NC_000022.10:g.19163698A>C , CM000684.1:g.19163698A>C	GRCh37
NC_000022.9:g.17543698A>C	NCBI36
NG_033863.1:g.7679T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.881T>G MANE Select	ENSP00000215882.5:p.Phe294Cys
ENST00000215882.9:c.881T>G	ENSP00000215882.5:p.Phe294Cys
ENST00000451283.5:c.572T>G	ENSP00000401480.1:p.Phe191Cys
ENST00000470922.5:n.1023T>G
NM_001256534.1:c.902T>G	NP_001243463.1:p.Phe301Cys
NM_001287387.1:c.572T>G	NP_001274316.1:p.Phe191Cys
NM_005984.4:c.881T>G	NP_005975.1:p.Phe294Cys
NR_046298.2:n.932T>G
NM_005984.5:c.881T>G MANE Select	NP_005975.1:p.Phe294Cys
NM_001256534.2:c.902T>G	NP_001243463.1:p.Phe301Cys
NM_001287387.2:c.572T>G	NP_001274316.1:p.Phe191Cys
NR_046298.3:n.805T>G