Canonical Allele Identifier: CA364718946

Gene: SLC17A5

Linked Data

• dbSNP Id: rs1581990197
• MyVariant Identifiers: chr6:g.74354203G>T (hg19) ; chr6:g.73644480G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73644480G>T , CM000668.2:g.73644480G>T	GRCh38
NC_000006.11:g.74354203G>T , CM000668.1:g.74354203G>T	GRCh37
NC_000006.10:g.74410924G>T	NCBI36
NG_008272.1:g.14535C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355773.6:c.218C>A MANE Select	ENSP00000348019.5:p.Thr73Asn
ENST00000355773.5:c.218C>A	ENSP00000348019.5:p.Thr73Asn
NM_012434.4:c.218C>A	NP_036566.1:p.Thr73Asn
XM_005248710.2:c.167C>A	XP_005248767.1:p.Thr56Asn
XM_005248711.1:c.20C>A	XP_005248768.1:p.Thr7Asn
XM_011535750.1:c.218C>A	XP_011534052.1:p.Thr73Asn
XM_011535751.1:c.218C>A	XP_011534053.1:p.Thr73Asn
NM_012434.5:c.218C>A MANE Select	NP_036566.1:p.Thr73Asn
NM_001382629.1:c.61-2556C>A	NP_001369558.1:n.61-2556C>A
NM_001382630.1:c.218C>A	NP_001369559.1:p.Thr73Asn
NM_001382631.1:c.239C>A	NP_001369560.1:p.Thr80Asn
NM_001382632.1:c.218C>A	NP_001369561.1:p.Thr73Asn
NM_001382633.1:c.218C>A	NP_001369562.1:p.Thr73Asn
NM_001382634.1:c.218C>A	NP_001369563.1:p.Thr73Asn
NM_001382635.1:c.218C>A	NP_001369564.1:p.Thr73Asn
NM_001382636.1:c.61-2556C>A	NP_001369565.1:n.61-2556C>A