Canonical Allele Identifier: CA410634391

Gene: SLC25A1

Linked Data

• gnomAD v4: 22-19176445-A-T
• MyVariant Identifiers: chr22:g.19163958A>T (hg19) ; chr22:g.19176445A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19176445A>T , CM000684.2:g.19176445A>T	GRCh38
NC_000022.10:g.19163958A>T , CM000684.1:g.19163958A>T	GRCh37
NC_000022.9:g.17543958A>T	NCBI36
NG_033863.1:g.7419T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.797T>A MANE Select	ENSP00000215882.5:p.Ile266Asn
ENST00000215882.9:c.797T>A	ENSP00000215882.5:p.Ile266Asn
ENST00000451283.5:c.488T>A	ENSP00000401480.1:p.Ile163Asn
ENST00000470922.5:n.939T>A
NM_001256534.1:c.818T>A	NP_001243463.1:p.Ile273Asn
NM_001287387.1:c.488T>A	NP_001274316.1:p.Ile163Asn
NM_005984.4:c.797T>A	NP_005975.1:p.Ile266Asn
NR_046298.2:n.848T>A
NM_005984.5:c.797T>A MANE Select	NP_005975.1:p.Ile266Asn
NM_001256534.2:c.818T>A	NP_001243463.1:p.Ile273Asn
NM_001287387.2:c.488T>A	NP_001274316.1:p.Ile163Asn
NR_046298.3:n.721T>A