Canonical Allele Identifier: CA410635887

Gene: SLC25A1

Linked Data

• dbSNP Id: rs781908532
• gnomAD v2: 22-19164098-C-A
• gnomAD v4: 22-19176585-C-A
• MyVariant Identifiers: chr22:g.19164098C>A (hg19) ; chr22:g.19176585C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19176585C>A , CM000684.2:g.19176585C>A	GRCh38
NC_000022.10:g.19164098C>A , CM000684.1:g.19164098C>A	GRCh37
NC_000022.9:g.17544098C>A	NCBI36
NG_033863.1:g.7279G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.740G>T MANE Select	ENSP00000215882.5:p.Arg247Leu
ENST00000215882.9:c.740G>T	ENSP00000215882.5:p.Arg247Leu
ENST00000451283.5:c.431G>T	ENSP00000401480.1:p.Arg144Leu
ENST00000470922.5:n.882G>T
NM_001256534.1:c.761G>T	NP_001243463.1:p.Arg254Leu
NM_001287387.1:c.431G>T	NP_001274316.1:p.Arg144Leu
NM_005984.4:c.740G>T	NP_005975.1:p.Arg247Leu
NR_046298.2:n.791G>T
NM_005984.5:c.740G>T MANE Select	NP_005975.1:p.Arg247Leu
NM_001256534.2:c.761G>T	NP_001243463.1:p.Arg254Leu
NM_001287387.2:c.431G>T	NP_001274316.1:p.Arg144Leu
NR_046298.3:n.664G>T