Canonical Allele Identifier: CA410634319

Gene: SLC25A1

Linked Data

• MyVariant Identifiers: chr22:g.19163950T>A (hg19) ; chr22:g.19176437T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19176437T>A , CM000684.2:g.19176437T>A	GRCh38
NC_000022.10:g.19163950T>A , CM000684.1:g.19163950T>A	GRCh37
NC_000022.9:g.17543950T>A	NCBI36
NG_033863.1:g.7427A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.805A>T MANE Select	ENSP00000215882.5:p.Lys269Ter
ENST00000215882.9:c.805A>T	ENSP00000215882.5:p.Lys269Ter
ENST00000451283.5:c.496A>T	ENSP00000401480.1:p.Lys166Ter
ENST00000470922.5:n.947A>T
NM_001256534.1:c.826A>T	NP_001243463.1:p.Lys276Ter
NM_001287387.1:c.496A>T	NP_001274316.1:p.Lys166Ter
NM_005984.4:c.805A>T	NP_005975.1:p.Lys269Ter
NR_046298.2:n.856A>T
NM_005984.5:c.805A>T MANE Select	NP_005975.1:p.Lys269Ter
NM_001256534.2:c.826A>T	NP_001243463.1:p.Lys276Ter
NM_001287387.2:c.496A>T	NP_001274316.1:p.Lys166Ter
NR_046298.3:n.729A>T