Canonical Allele Identifier: CA364713547

Gene: SLC17A5

Linked Data

• MyVariant Identifiers: chr6:g.74331610A>C (hg19) ; chr6:g.73621887A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73621887A>C , CM000668.2:g.73621887A>C	GRCh38
NC_000006.11:g.74331610A>C , CM000668.1:g.74331610A>C	GRCh37
NC_000006.10:g.74388331A>C	NCBI36
NG_008272.1:g.37128T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000355773.6:c.895T>G MANE Select	ENSP00000348019.5:p.Phe299Val
ENST00000355773.5:c.895T>G	ENSP00000348019.5:p.Phe299Val
NM_012434.4:c.895T>G	NP_036566.1:p.Phe299Val
XM_005248710.2:c.844T>G	XP_005248767.1:p.Phe282Val
XM_005248711.1:c.697T>G	XP_005248768.1:p.Phe233Val
XM_011535750.1:c.895T>G	XP_011534052.1:p.Phe299Val
NM_012434.5:c.895T>G MANE Select	NP_036566.1:p.Phe299Val
NM_001382629.1:c.664T>G	NP_001369558.1:p.Phe222Val
NM_001382630.1:c.895T>G	NP_001369559.1:p.Phe299Val
NM_001382631.1:c.916T>G	NP_001369560.1:p.Phe306Val
NM_001382632.1:c.808T>G	NP_001369561.1:p.Phe270Val
NM_001382633.1:c.895T>G	NP_001369562.1:p.Phe299Val
NM_001382634.1:c.820-6440T>G	NP_001369563.1:n.820-6440T>G
NM_001382635.1:c.892T>G	NP_001369564.1:p.Phe298Val
NM_001382636.1:c.577T>G	NP_001369565.1:p.Phe193Val