Canonical Allele Identifier: CA827949151

Gene: SLC17A5

Linked Data

• dbSNP Id: rs959444920
• gnomAD v3: 6-73600236-A-C
• gnomAD v4: 6-73600236-A-C
• MyVariant Identifiers: chr6:g.74309959A>C (hg19) ; chr6:g.73600236A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73600236A>C , CM000668.2:g.73600236A>C	GRCh38
NC_000006.11:g.74309959A>C , CM000668.1:g.74309959A>C	GRCh37
NC_000006.10:g.74366680A>C	NCBI36
NG_008272.1:g.58779T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355773.6:c.1350+115T>G MANE Select	ENSP00000348019.5:n.1350+115T>G
ENST00000355773.5:c.1350+115T>G	ENSP00000348019.5:n.1350+115T>G
NM_012434.4:c.1350+115T>G	NP_036566.1:n.1350+115T>G
XM_005248710.2:c.1299+115T>G	XP_005248767.1:n.1299+115T>G
XM_005248711.1:c.1152+115T>G	XP_005248768.1:n.1152+115T>G
XM_011535750.1:c.*8+115T>G	XP_011534052.1:n.*8+115T>G
NM_012434.5:c.1350+115T>G MANE Select	NP_036566.1:n.1350+115T>G
NM_001382629.1:c.1119+115T>G	NP_001369558.1:n.1119+115T>G
NM_001382630.1:c.1260-5022T>G	NP_001369559.1:n.1260-5022T>G
NM_001382631.1:c.1371+115T>G	NP_001369560.1:n.1371+115T>G
NM_001382632.1:c.1263+115T>G	NP_001369561.1:n.1263+115T>G
NM_001382633.1:c.1350+115T>G	NP_001369562.1:n.1350+115T>G
NM_001382634.1:c.1191+115T>G	NP_001369563.1:n.1191+115T>G
NM_001382635.1:c.1347+115T>G	NP_001369564.1:n.1347+115T>G
NM_001382636.1:c.1032+115T>G	NP_001369565.1:n.1032+115T>G