Canonical Allele Identifier: CA1087052688
Gene: SLC17A3 HGNC NCBI

Linked Data

dbSNP Id: rs1473453397
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.25869051T>G , CM000668.2:g.25869051T>G GRCh38
NC_000006.11:g.25869279T>G , CM000668.1:g.25869279T>G GRCh37
NC_000006.10:g.25977258T>G NCBI36
NG_032922.1:g.10193A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360657.7:c.-33-631A>C ENSP00000353873.3:n.-33-631A>C
ENST00000361703.10:c.-33-631A>C ENSP00000355307.6:n.-33-631A>C
ENST00000397060.8:c.-33-631A>C MANE Select ENSP00000380250.4:n.-33-631A>C
ENST00000503922.5:n.73-631A>C
ENST00000506105.5:c.-33-631A>C ENSP00000424729.1:n.-33-631A>C
NM_001098486.1:c.-33-631A>C NP_001091956.1:n.-33-631A>C
NM_006632.3:c.-33-631A>C NP_006623.2:n.-33-631A>C
NM_001098486.2:c.-33-631A>C MANE Select NP_001091956.1:n.-33-631A>C
NM_006632.4:c.-33-631A>C NP_006623.2:n.-33-631A>C
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