Canonical Allele Identifier: CA410635356

Gene: SLC25A1

Linked Data

• gnomAD v4: 22-19176467-T-G
• MyVariant Identifiers: chr22:g.19163980T>G (hg19) ; chr22:g.19176467T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19176467T>G , CM000684.2:g.19176467T>G	GRCh38
NC_000022.10:g.19163980T>G , CM000684.1:g.19163980T>G	GRCh37
NC_000022.9:g.17543980T>G	NCBI36
NG_033863.1:g.7397A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.775A>C MANE Select	ENSP00000215882.5:p.Thr259Pro
ENST00000215882.9:c.775A>C	ENSP00000215882.5:p.Thr259Pro
ENST00000451283.5:c.466A>C	ENSP00000401480.1:p.Thr156Pro
ENST00000470922.5:n.917A>C
NM_001256534.1:c.796A>C	NP_001243463.1:p.Thr266Pro
NM_001287387.1:c.466A>C	NP_001274316.1:p.Thr156Pro
NM_005984.4:c.775A>C	NP_005975.1:p.Thr259Pro
NR_046298.2:n.826A>C
NM_005984.5:c.775A>C MANE Select	NP_005975.1:p.Thr259Pro
NM_001256534.2:c.796A>C	NP_001243463.1:p.Thr266Pro
NM_001287387.2:c.466A>C	NP_001274316.1:p.Thr156Pro
NR_046298.3:n.699A>C