Canonical Allele Identifier: CA410636614
Gene: SLC25A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176663A>G , CM000684.2:g.19176663A>G GRCh38
NC_000022.10:g.19164176A>G , CM000684.1:g.19164176A>G GRCh37
NC_000022.9:g.17544176A>G NCBI36
NG_033863.1:g.7201T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000215882.10:c.662T>C MANE Select ENSP00000215882.5:p.Leu221Pro
ENST00000215882.9:c.662T>C ENSP00000215882.5:p.Leu221Pro
ENST00000451283.5:c.353T>C ENSP00000401480.1:p.Leu118Pro
ENST00000470922.5:n.804T>C
NM_001256534.1:c.683T>C NP_001243463.1:p.Leu228Pro
NM_001287387.1:c.353T>C NP_001274316.1:p.Leu118Pro
NM_005984.4:c.662T>C NP_005975.1:p.Leu221Pro
NR_046298.2:n.713T>C
NM_005984.5:c.662T>C MANE Select NP_005975.1:p.Leu221Pro
NM_001256534.2:c.683T>C NP_001243463.1:p.Leu228Pro
NM_001287387.2:c.353T>C NP_001274316.1:p.Leu118Pro
NR_046298.3:n.586T>C