Canonical Allele Identifier: CA410633769

Gene: SLC25A1

Linked Data

• MyVariant Identifiers: chr22:g.19163699A>T (hg19) ; chr22:g.19176186A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19176186A>T , CM000684.2:g.19176186A>T	GRCh38
NC_000022.10:g.19163699A>T , CM000684.1:g.19163699A>T	GRCh37
NC_000022.9:g.17543699A>T	NCBI36
NG_033863.1:g.7678T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.880T>A MANE Select	ENSP00000215882.5:p.Phe294Ile
ENST00000215882.9:c.880T>A	ENSP00000215882.5:p.Phe294Ile
ENST00000451283.5:c.571T>A	ENSP00000401480.1:p.Phe191Ile
ENST00000470922.5:n.1022T>A
NM_001256534.1:c.901T>A	NP_001243463.1:p.Phe301Ile
NM_001287387.1:c.571T>A	NP_001274316.1:p.Phe191Ile
NM_005984.4:c.880T>A	NP_005975.1:p.Phe294Ile
NR_046298.2:n.931T>A
NM_005984.5:c.880T>A MANE Select	NP_005975.1:p.Phe294Ile
NM_001256534.2:c.901T>A	NP_001243463.1:p.Phe301Ile
NM_001287387.2:c.571T>A	NP_001274316.1:p.Phe191Ile
NR_046298.3:n.804T>A