Canonical Allele Identifier: CA364719940

Gene: SLC17A5

Linked Data

• MyVariant Identifiers: chr6:g.74310082T>G (hg19) ; chr6:g.73600359T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73600359T>G , CM000668.2:g.73600359T>G	GRCh38
NC_000006.11:g.74310082T>G , CM000668.1:g.74310082T>G	GRCh37
NC_000006.10:g.74366803T>G	NCBI36
NG_008272.1:g.58656A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355773.6:c.1342A>C MANE Select	ENSP00000348019.5:p.Thr448Pro
ENST00000355773.5:c.1342A>C	ENSP00000348019.5:p.Thr448Pro
NM_012434.4:c.1342A>C	NP_036566.1:p.Thr448Pro
XM_005248710.2:c.1291A>C	XP_005248767.1:p.Thr431Pro
XM_005248711.1:c.1144A>C	XP_005248768.1:p.Thr382Pro
XM_011535750.1:c.1194A>C	XP_011534052.1:p.Ter398Cys
NM_012434.5:c.1342A>C MANE Select	NP_036566.1:p.Thr448Pro
NM_001382629.1:c.1111A>C	NP_001369558.1:p.Thr371Pro
NM_001382630.1:c.1260-5145A>C	NP_001369559.1:n.1260-5145A>C
NM_001382631.1:c.1363A>C	NP_001369560.1:p.Thr455Pro
NM_001382632.1:c.1255A>C	NP_001369561.1:p.Thr419Pro
NM_001382633.1:c.1342A>C	NP_001369562.1:p.Thr448Pro
NM_001382634.1:c.1183A>C	NP_001369563.1:p.Thr395Pro
NM_001382635.1:c.1339A>C	NP_001369564.1:p.Thr447Pro
NM_001382636.1:c.1024A>C	NP_001369565.1:p.Thr342Pro