Canonical Allele Identifier: CA1638223888

Gene: SLC17A5

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73600401T= , CM000668.2:g.73600401T=	GRCh38
NC_000006.11:g.74310124T= , CM000668.1:g.74310124T=	GRCh37
NC_000006.10:g.74366845T=	NCBI36
NG_008272.1:g.58614A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355773.6:c.1300A= MANE Select	ENSP00000348019.5:p.Thr434=
ENST00000355773.5:c.1300A=	ENSP00000348019.5:p.Thr434=
NM_012434.4:c.1300A=	NP_036566.1:p.Thr434=
XM_005248710.2:c.1249A=	XP_005248767.1:p.Thr417=
XM_005248711.1:c.1102A=	XP_005248768.1:p.Thr368=
XM_011535750.1:c.1152A=	XP_011534052.1:p.Pro384=
NM_012434.5:c.1300A= MANE Select	NP_036566.1:p.Thr434=
NM_001382629.1:c.1069A=	NP_001369558.1:p.Thr357=
NM_001382630.1:c.1260-5187A=	NP_001369559.1:n.1260-5187A=
NM_001382631.1:c.1321A=	NP_001369560.1:p.Thr441=
NM_001382632.1:c.1213A=	NP_001369561.1:p.Thr405=
NM_001382633.1:c.1300A=	NP_001369562.1:p.Thr434=
NM_001382634.1:c.1141A=	NP_001369563.1:p.Thr381=
NM_001382635.1:c.1297A=	NP_001369564.1:p.Thr433=
NM_001382636.1:c.982A=	NP_001369565.1:p.Thr328=