Canonical Allele Identifier: CA1616789255
Gene: SLC17A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.25869111G= , CM000668.2:g.25869111G= GRCh38
NC_000006.11:g.25869339G= , CM000668.1:g.25869339G= GRCh37
NC_000006.10:g.25977318G= NCBI36
NG_032922.1:g.10133C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360657.7:c.-33-691C= ENSP00000353873.3:n.-33-691C=
ENST00000361703.10:c.-33-691C= ENSP00000355307.6:n.-33-691C=
ENST00000397060.8:c.-33-691C= MANE Select ENSP00000380250.4:n.-33-691C=
ENST00000503922.5:n.73-691C=
ENST00000506105.5:c.-33-691C= ENSP00000424729.1:n.-33-691C=
NM_001098486.1:c.-33-691C= NP_001091956.1:n.-33-691C=
NM_006632.3:c.-33-691C= NP_006623.2:n.-33-691C=
NM_001098486.2:c.-33-691C= MANE Select NP_001091956.1:n.-33-691C=
NM_006632.4:c.-33-691C= NP_006623.2:n.-33-691C=