Canonical Allele Identifier: CA1616789272
Gene: SLC17A3 HGNC NCBI

Linked Data

dbSNP Id: rs1765597541

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.25869162G>A , CM000668.2:g.25869162G>A GRCh38
NC_000006.11:g.25869390G>A , CM000668.1:g.25869390G>A GRCh37
NC_000006.10:g.25977369G>A NCBI36
NG_032922.1:g.10082C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360657.7:c.-33-742C>T ENSP00000353873.3:n.-33-742C>T
ENST00000361703.10:c.-33-742C>T ENSP00000355307.6:n.-33-742C>T
ENST00000397060.8:c.-33-742C>T MANE Select ENSP00000380250.4:n.-33-742C>T
ENST00000503922.5:n.73-742C>T
ENST00000506105.5:c.-33-742C>T ENSP00000424729.1:n.-33-742C>T
NM_001098486.1:c.-33-742C>T NP_001091956.1:n.-33-742C>T
NM_006632.3:c.-33-742C>T NP_006623.2:n.-33-742C>T
NM_001098486.2:c.-33-742C>T MANE Select NP_001091956.1:n.-33-742C>T
NM_006632.4:c.-33-742C>T NP_006623.2:n.-33-742C>T