Canonical Allele Identifier: CA321343735

Gene: SLC25A1

Linked Data

• dbSNP Id: rs1022759287
• MyVariant Identifiers: chr22:g.19163786A>C (hg19) ; chr22:g.19176273A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19176273A>C , CM000684.2:g.19176273A>C	GRCh38
NC_000022.10:g.19163786A>C , CM000684.1:g.19163786A>C	GRCh37
NC_000022.9:g.17543786A>C	NCBI36
NG_033863.1:g.7591T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.822-29T>G MANE Select	ENSP00000215882.5:n.822-29T>G
ENST00000215882.9:c.822-29T>G	ENSP00000215882.5:n.822-29T>G
ENST00000451283.5:c.513-29T>G	ENSP00000401480.1:n.513-29T>G
ENST00000470922.5:n.964-29T>G
NM_001256534.1:c.843-29T>G	NP_001243463.1:n.843-29T>G
NM_001287387.1:c.513-29T>G	NP_001274316.1:n.513-29T>G
NM_005984.4:c.822-29T>G	NP_005975.1:n.822-29T>G
NR_046298.2:n.873-29T>G
NM_005984.5:c.822-29T>G MANE Select	NP_005975.1:n.822-29T>G
NM_001256534.2:c.843-29T>G	NP_001243463.1:n.843-29T>G
NM_001287387.2:c.513-29T>G	NP_001274316.1:n.513-29T>G
NR_046298.3:n.746-29T>G