Canonical Allele Identifier: CA410633822

Gene: SLC25A1

Linked Data

• dbSNP Id: rs1470275081
• gnomAD v3: 22-19176194-G-A
• gnomAD v4: 22-19176194-G-A
• MyVariant Identifiers: chr22:g.19163707G>A (hg19) ; chr22:g.19176194G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19176194G>A , CM000684.2:g.19176194G>A	GRCh38
NC_000022.10:g.19163707G>A , CM000684.1:g.19163707G>A	GRCh37
NC_000022.9:g.17543707G>A	NCBI36
NG_033863.1:g.7670C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.872C>T MANE Select	ENSP00000215882.5:p.Ala291Val
ENST00000215882.9:c.872C>T	ENSP00000215882.5:p.Ala291Val
ENST00000451283.5:c.563C>T	ENSP00000401480.1:p.Ala188Val
ENST00000470922.5:n.1014C>T
NM_001256534.1:c.893C>T	NP_001243463.1:p.Ala298Val
NM_001287387.1:c.563C>T	NP_001274316.1:p.Ala188Val
NM_005984.4:c.872C>T	NP_005975.1:p.Ala291Val
NR_046298.2:n.923C>T
NM_005984.5:c.872C>T MANE Select	NP_005975.1:p.Ala291Val
NM_001256534.2:c.893C>T	NP_001243463.1:p.Ala298Val
NM_001287387.2:c.563C>T	NP_001274316.1:p.Ala188Val
NR_046298.3:n.796C>T