Canonical Allele Identifier: CA513188096

Gene: SLC25A1

Linked Data

• MyVariant Identifiers: chr22:g.19164399G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19176886G>T , CM000684.2:g.19176886G>T	GRCh38
NC_000022.10:g.19164399G>T , CM000684.1:g.19164399G>T	GRCh37
NC_000022.9:g.17544399G>T	NCBI36
NG_033863.1:g.6978C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.591C>A MANE Select	ENSP00000215882.5:p.Ile197=
ENST00000215882.9:c.591C>A	ENSP00000215882.5:p.Ile197=
ENST00000451283.5:c.282C>A	ENSP00000401480.1:p.Ile94=
ENST00000461267.1:n.737C>A
ENST00000470922.5:n.733C>A
NM_001256534.1:c.612C>A	NP_001243463.1:p.Ile204=
NM_001287387.1:c.282C>A	NP_001274316.1:p.Ile94=
NM_005984.4:c.591C>A	NP_005975.1:p.Ile197=
NR_046298.2:n.642C>A
NM_005984.5:c.591C>A MANE Select	NP_005975.1:p.Ile197=
NM_001256534.2:c.612C>A	NP_001243463.1:p.Ile204=
NM_001287387.2:c.282C>A	NP_001274316.1:p.Ile94=
NR_046298.3:n.515C>A