Canonical Allele Identifier: CA513188110

Gene: SLC25A1

Linked Data

• MyVariant Identifiers: chr22:g.19164425G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19176912G>A , CM000684.2:g.19176912G>A	GRCh38
NC_000022.10:g.19164425G>A , CM000684.1:g.19164425G>A	GRCh37
NC_000022.9:g.17544425G>A	NCBI36
NG_033863.1:g.6952C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.565C>T MANE Select	ENSP00000215882.5:p.Leu189=
ENST00000215882.9:c.565C>T	ENSP00000215882.5:p.Leu189=
ENST00000451283.5:c.256C>T	ENSP00000401480.1:p.Leu86=
ENST00000461267.1:n.711C>T
ENST00000470922.5:n.707C>T
NM_001256534.1:c.586C>T	NP_001243463.1:p.Leu196=
NM_001287387.1:c.256C>T	NP_001274316.1:p.Leu86=
NM_005984.4:c.565C>T	NP_005975.1:p.Leu189=
NR_046298.2:n.616C>T
NM_005984.5:c.565C>T MANE Select	NP_005975.1:p.Leu189=
NM_001256534.2:c.586C>T	NP_001243463.1:p.Leu196=
NM_001287387.2:c.256C>T	NP_001274316.1:p.Leu86=
NR_046298.3:n.489C>T