Canonical Allele Identifier: CA2395757878
Gene: SLC25A1 HGNC NCBI

Linked Data

dbSNP Id: rs1601397387

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176113T>C , CM000684.2:g.19176113T>C GRCh38
NC_000022.10:g.19163626T>C , CM000684.1:g.19163626T>C GRCh37
NC_000022.9:g.17543626T>C NCBI36
NG_033863.1:g.7751A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.*17A>G MANE Select ENSP00000215882.5:n.*17A>G
ENST00000215882.9:c.*17A>G ENSP00000215882.5:n.*17A>G
ENST00000451283.5:c.*17A>G ENSP00000401480.1:n.*17A>G
ENST00000470922.5:n.1095A>G
NM_001256534.1:c.*17A>G NP_001243463.1:n.*17A>G
NM_001287387.1:c.*17A>G NP_001274316.1:n.*17A>G
NM_005984.4:c.*17A>G NP_005975.1:n.*17A>G
NR_046298.2:n.1004A>G
NM_005984.5:c.*17A>G MANE Select NP_005975.1:n.*17A>G
NM_001256534.2:c.*17A>G NP_001243463.1:n.*17A>G
NM_001287387.2:c.*17A>G NP_001274316.1:n.*17A>G
NR_046298.3:n.877A>G