Canonical Allele Identifier: CA410636106

Gene: SLC25A1

Linked Data

• MyVariant Identifiers: chr22:g.19164122G>A (hg19) ; chr22:g.19176609G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19176609G>A , CM000684.2:g.19176609G>A	GRCh38
NC_000022.10:g.19164122G>A , CM000684.1:g.19164122G>A	GRCh37
NC_000022.9:g.17544122G>A	NCBI36
NG_033863.1:g.7255C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.716C>T MANE Select	ENSP00000215882.5:p.Thr239Ile
ENST00000215882.9:c.716C>T	ENSP00000215882.5:p.Thr239Ile
ENST00000451283.5:c.407C>T	ENSP00000401480.1:p.Thr136Ile
ENST00000470922.5:n.858C>T
NM_001256534.1:c.737C>T	NP_001243463.1:p.Thr246Ile
NM_001287387.1:c.407C>T	NP_001274316.1:p.Thr136Ile
NM_005984.4:c.716C>T	NP_005975.1:p.Thr239Ile
NR_046298.2:n.767C>T
NM_005984.5:c.716C>T MANE Select	NP_005975.1:p.Thr239Ile
NM_001256534.2:c.737C>T	NP_001243463.1:p.Thr246Ile
NM_001287387.2:c.407C>T	NP_001274316.1:p.Thr136Ile
NR_046298.3:n.640C>T