Canonical Allele Identifier: CA364719933

Gene: SLC17A5

Linked Data

• MyVariant Identifiers: chr6:g.74310079G>T (hg19) ; chr6:g.73600356G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73600356G>T , CM000668.2:g.73600356G>T	GRCh38
NC_000006.11:g.74310079G>T , CM000668.1:g.74310079G>T	GRCh37
NC_000006.10:g.74366800G>T	NCBI36
NG_008272.1:g.58659C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355773.6:c.1345C>A MANE Select	ENSP00000348019.5:p.Pro449Thr
ENST00000355773.5:c.1345C>A	ENSP00000348019.5:p.Pro449Thr
NM_012434.4:c.1345C>A	NP_036566.1:p.Pro449Thr
XM_005248710.2:c.1294C>A	XP_005248767.1:p.Pro432Thr
XM_005248711.1:c.1147C>A	XP_005248768.1:p.Pro383Thr
XM_011535750.1:c.*3C>A	XP_011534052.1:n.*3C>A
NM_012434.5:c.1345C>A MANE Select	NP_036566.1:p.Pro449Thr
NM_001382629.1:c.1114C>A	NP_001369558.1:p.Pro372Thr
NM_001382630.1:c.1260-5142C>A	NP_001369559.1:n.1260-5142C>A
NM_001382631.1:c.1366C>A	NP_001369560.1:p.Pro456Thr
NM_001382632.1:c.1258C>A	NP_001369561.1:p.Pro420Thr
NM_001382633.1:c.1345C>A	NP_001369562.1:p.Pro449Thr
NM_001382634.1:c.1186C>A	NP_001369563.1:p.Pro396Thr
NM_001382635.1:c.1342C>A	NP_001369564.1:p.Pro448Thr
NM_001382636.1:c.1027C>A	NP_001369565.1:p.Pro343Thr