Canonical Allele Identifier: CA512978320

Gene: SLC25A1

Linked Data

• MyVariant Identifiers: chr22:g.19163706G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19176193G>C , CM000684.2:g.19176193G>C	GRCh38
NC_000022.10:g.19163706G>C , CM000684.1:g.19163706G>C	GRCh37
NC_000022.9:g.17543706G>C	NCBI36
NG_033863.1:g.7671C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.873C>G MANE Select	ENSP00000215882.5:p.Ala291=
ENST00000215882.9:c.873C>G	ENSP00000215882.5:p.Ala291=
ENST00000451283.5:c.564C>G	ENSP00000401480.1:p.Ala188=
ENST00000470922.5:n.1015C>G
NM_001256534.1:c.894C>G	NP_001243463.1:p.Ala298=
NM_001287387.1:c.564C>G	NP_001274316.1:p.Ala188=
NM_005984.4:c.873C>G	NP_005975.1:p.Ala291=
NR_046298.2:n.924C>G
NM_005984.5:c.873C>G MANE Select	NP_005975.1:p.Ala291=
NM_001256534.2:c.894C>G	NP_001243463.1:p.Ala298=
NM_001287387.2:c.564C>G	NP_001274316.1:p.Ala188=
NR_046298.3:n.797C>G