Canonical Allele Identifier: CA364719989

Gene: SLC17A5

Linked Data

• MyVariant Identifiers: chr6:g.74310108A>C (hg19) ; chr6:g.73600385A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73600385A>C , CM000668.2:g.73600385A>C	GRCh38
NC_000006.11:g.74310108A>C , CM000668.1:g.74310108A>C	GRCh37
NC_000006.10:g.74366829A>C	NCBI36
NG_008272.1:g.58630T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355773.6:c.1316T>G MANE Select	ENSP00000348019.5:p.Val439Gly
ENST00000355773.5:c.1316T>G	ENSP00000348019.5:p.Val439Gly
NM_012434.4:c.1316T>G	NP_036566.1:p.Val439Gly
XM_005248710.2:c.1265T>G	XP_005248767.1:p.Val422Gly
XM_005248711.1:c.1118T>G	XP_005248768.1:p.Val373Gly
XM_011535750.1:c.1168T>G	XP_011534052.1:p.Leu390Val
NM_012434.5:c.1316T>G MANE Select	NP_036566.1:p.Val439Gly
NM_001382629.1:c.1085T>G	NP_001369558.1:p.Val362Gly
NM_001382630.1:c.1260-5171T>G	NP_001369559.1:n.1260-5171T>G
NM_001382631.1:c.1337T>G	NP_001369560.1:p.Val446Gly
NM_001382632.1:c.1229T>G	NP_001369561.1:p.Val410Gly
NM_001382633.1:c.1316T>G	NP_001369562.1:p.Val439Gly
NM_001382634.1:c.1157T>G	NP_001369563.1:p.Val386Gly
NM_001382635.1:c.1313T>G	NP_001369564.1:p.Val438Gly
NM_001382636.1:c.998T>G	NP_001369565.1:p.Val333Gly