Canonical Allele Identifier: CA410636714

Gene: SLC25A1

Linked Data

• MyVariant Identifiers: chr22:g.19164192T>C (hg19) ; chr22:g.19176679T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19176679T>C , CM000684.2:g.19176679T>C	GRCh38
NC_000022.10:g.19164192T>C , CM000684.1:g.19164192T>C	GRCh37
NC_000022.9:g.17544192T>C	NCBI36
NG_033863.1:g.7185A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.646A>G MANE Select	ENSP00000215882.5:p.Lys216Glu
ENST00000215882.9:c.646A>G	ENSP00000215882.5:p.Lys216Glu
ENST00000451283.5:c.337A>G	ENSP00000401480.1:p.Lys113Glu
ENST00000461267.1:n.792A>G
ENST00000470922.5:n.788A>G
NM_001256534.1:c.667A>G	NP_001243463.1:p.Lys223Glu
NM_001287387.1:c.337A>G	NP_001274316.1:p.Lys113Glu
NM_005984.4:c.646A>G	NP_005975.1:p.Lys216Glu
NR_046298.2:n.697A>G
NM_005984.5:c.646A>G MANE Select	NP_005975.1:p.Lys216Glu
NM_001256534.2:c.667A>G	NP_001243463.1:p.Lys223Glu
NM_001287387.2:c.337A>G	NP_001274316.1:p.Lys113Glu
NR_046298.3:n.570A>G