Canonical Allele Identifier: CA364717888

Gene: SLC17A5

Linked Data

• MyVariant Identifiers: chr6:g.74351436C>A (hg19) ; chr6:g.73641713C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73641713C>A , CM000668.2:g.73641713C>A	GRCh38
NC_000006.11:g.74351436C>A , CM000668.1:g.74351436C>A	GRCh37
NC_000006.10:g.74408157C>A	NCBI36
NG_008272.1:g.17302G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000355773.6:c.503G>T MANE Select	ENSP00000348019.5:p.Arg168Ile
ENST00000355773.5:c.503G>T	ENSP00000348019.5:p.Arg168Ile
ENST00000481996.1:n.269G>T
NM_012434.4:c.503G>T	NP_036566.1:p.Arg168Ile
XM_005248710.2:c.452G>T	XP_005248767.1:p.Arg151Ile
XM_005248711.1:c.305G>T	XP_005248768.1:p.Arg102Ile
XM_011535750.1:c.503G>T	XP_011534052.1:p.Arg168Ile
XM_011535751.1:c.503G>T	XP_011534053.1:p.Arg168Ile
NM_012434.5:c.503G>T MANE Select	NP_036566.1:p.Arg168Ile
NM_001382629.1:c.272G>T	NP_001369558.1:p.Arg91Ile
NM_001382630.1:c.503G>T	NP_001369559.1:p.Arg168Ile
NM_001382631.1:c.524G>T	NP_001369560.1:p.Arg175Ile
NM_001382632.1:c.503G>T	NP_001369561.1:p.Arg168Ile
NM_001382633.1:c.503G>T	NP_001369562.1:p.Arg168Ile
NM_001382634.1:c.503G>T	NP_001369563.1:p.Arg168Ile
NM_001382635.1:c.503G>T	NP_001369564.1:p.Arg168Ile
NM_001382636.1:c.272G>T	NP_001369565.1:p.Arg91Ile