Canonical Allele Identifier: CA364719971

Gene: SLC17A5

Linked Data

• MyVariant Identifiers: chr6:g.74310097T>A (hg19) ; chr6:g.73600374T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73600374T>A , CM000668.2:g.73600374T>A	GRCh38
NC_000006.11:g.74310097T>A , CM000668.1:g.74310097T>A	GRCh37
NC_000006.10:g.74366818T>A	NCBI36
NG_008272.1:g.58641A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355773.6:c.1327A>T MANE Select	ENSP00000348019.5:p.Ile443Phe
ENST00000355773.5:c.1327A>T	ENSP00000348019.5:p.Ile443Phe
NM_012434.4:c.1327A>T	NP_036566.1:p.Ile443Phe
XM_005248710.2:c.1276A>T	XP_005248767.1:p.Ile426Phe
XM_005248711.1:c.1129A>T	XP_005248768.1:p.Ile377Phe
XM_011535750.1:c.1179A>T	XP_011534052.1:p.Ser393=
NM_012434.5:c.1327A>T MANE Select	NP_036566.1:p.Ile443Phe
NM_001382629.1:c.1096A>T	NP_001369558.1:p.Ile366Phe
NM_001382630.1:c.1260-5160A>T	NP_001369559.1:n.1260-5160A>T
NM_001382631.1:c.1348A>T	NP_001369560.1:p.Ile450Phe
NM_001382632.1:c.1240A>T	NP_001369561.1:p.Ile414Phe
NM_001382633.1:c.1327A>T	NP_001369562.1:p.Ile443Phe
NM_001382634.1:c.1168A>T	NP_001369563.1:p.Ile390Phe
NM_001382635.1:c.1324A>T	NP_001369564.1:p.Ile442Phe
NM_001382636.1:c.1009A>T	NP_001369565.1:p.Ile337Phe