Canonical Allele Identifier: CA2655256446

Gene: SLC25A1

Linked Data

• gnomAD v4: 22-19177609-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19177609C>T , CM000684.2:g.19177609C>T	GRCh38
NC_000022.10:g.19165122C>T , CM000684.1:g.19165122C>T	GRCh37
NC_000022.9:g.17545122C>T	NCBI36
NG_033805.1:g.119108G>A
NG_033863.1:g.6255G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.441+118G>A MANE Select	ENSP00000215882.5:n.441+118G>A
ENST00000215882.9:c.441+118G>A	ENSP00000215882.5:n.441+118G>A
ENST00000451283.5:c.132+118G>A	ENSP00000401480.1:n.132+118G>A
ENST00000461267.1:n.587+118G>A
ENST00000470922.5:n.583+118G>A
NM_001256534.1:c.462+118G>A	NP_001243463.1:n.462+118G>A
NM_001287387.1:c.132+118G>A	NP_001274316.1:n.132+118G>A
NM_005984.4:c.441+118G>A	NP_005975.1:n.441+118G>A
NR_046298.2:n.492+333G>A
NM_005984.5:c.441+118G>A MANE Select	NP_005975.1:n.441+118G>A
NM_001256534.2:c.462+118G>A	NP_001243463.1:n.462+118G>A
NM_001287387.2:c.132+118G>A	NP_001274316.1:n.132+118G>A
NR_046298.3:n.365+333G>A