Canonical Allele Identifier: CA410634269

Gene: SLC25A1

Linked Data

• dbSNP Id: rs1555922291
• gnomAD v4: 22-19176431-C-T
• MyVariant Identifiers: chr22:g.19163944C>T (hg19) ; chr22:g.19176431C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19176431C>T , CM000684.2:g.19176431C>T	GRCh38
NC_000022.10:g.19163944C>T , CM000684.1:g.19163944C>T	GRCh37
NC_000022.9:g.17543944C>T	NCBI36
NG_033863.1:g.7433G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.811G>A MANE Select	ENSP00000215882.5:p.Gly271Arg
ENST00000215882.9:c.811G>A	ENSP00000215882.5:p.Gly271Arg
ENST00000451283.5:c.502G>A	ENSP00000401480.1:p.Gly168Arg
ENST00000470922.5:n.953G>A
NM_001256534.1:c.832G>A	NP_001243463.1:p.Gly278Arg
NM_001287387.1:c.502G>A	NP_001274316.1:p.Gly168Arg
NM_005984.4:c.811G>A	NP_005975.1:p.Gly271Arg
NR_046298.2:n.862G>A
NM_005984.5:c.811G>A MANE Select	NP_005975.1:p.Gly271Arg
NM_001256534.2:c.832G>A	NP_001243463.1:p.Gly278Arg
NM_001287387.2:c.502G>A	NP_001274316.1:p.Gly168Arg
NR_046298.3:n.735G>A