Canonical Allele Identifier: CA513188090

Gene: SLC25A1

Linked Data

• MyVariant Identifiers: chr22:g.19164387G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19176874G>T , CM000684.2:g.19176874G>T	GRCh38
NC_000022.10:g.19164387G>T , CM000684.1:g.19164387G>T	GRCh37
NC_000022.9:g.17544387G>T	NCBI36
NG_033863.1:g.6990C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.603C>A MANE Select	ENSP00000215882.5:p.Val201=
ENST00000215882.9:c.603C>A	ENSP00000215882.5:p.Val201=
ENST00000451283.5:c.294C>A	ENSP00000401480.1:p.Val98=
ENST00000461267.1:n.749C>A
ENST00000470922.5:n.745C>A
NM_001256534.1:c.624C>A	NP_001243463.1:p.Val208=
NM_001287387.1:c.294C>A	NP_001274316.1:p.Val98=
NM_005984.4:c.603C>A	NP_005975.1:p.Val201=
NR_046298.2:n.654C>A
NM_005984.5:c.603C>A MANE Select	NP_005975.1:p.Val201=
NM_001256534.2:c.624C>A	NP_001243463.1:p.Val208=
NM_001287387.2:c.294C>A	NP_001274316.1:p.Val98=
NR_046298.3:n.527C>A