Canonical Allele Identifier: CA10097236
Gene: SLC25A1 HGNC NCBI

Linked Data

dbSNP Id: rs782814974
ExAC: 22:19163634 T / C
gnomAD v2: 22-19163634-T-C
gnomAD v3: 22-19176121-T-C
gnomAD v4: 22-19176121-T-C
MyVariant Identifiers: chr22:g.19163634T>C (hg19) chr22:g.19176121T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176121T>C , CM000684.2:g.19176121T>C GRCh38
NC_000022.10:g.19163634T>C , CM000684.1:g.19163634T>C GRCh37
NC_000022.9:g.17543634T>C NCBI36
NG_033863.1:g.7743A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.*9A>G MANE Select ENSP00000215882.5:n.*9A>G
ENST00000215882.9:c.*9A>G ENSP00000215882.5:n.*9A>G
ENST00000451283.5:c.*9A>G ENSP00000401480.1:n.*9A>G
ENST00000470922.5:n.1087A>G
NM_001256534.1:c.*9A>G NP_001243463.1:n.*9A>G
NM_001287387.1:c.*9A>G NP_001274316.1:n.*9A>G
NM_005984.4:c.*9A>G NP_005975.1:n.*9A>G
NR_046298.2:n.996A>G
NM_005984.5:c.*9A>G MANE Select NP_005975.1:n.*9A>G
NM_001256534.2:c.*9A>G NP_001243463.1:n.*9A>G
NM_001287387.2:c.*9A>G NP_001274316.1:n.*9A>G
NR_046298.3:n.869A>G
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