Canonical Allele Identifier: CA1638223799

Gene: SLC17A5

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73600352T= , CM000668.2:g.73600352T=	GRCh38
NC_000006.11:g.74310075T= , CM000668.1:g.74310075T=	GRCh37
NC_000006.10:g.74366796T=	NCBI36
NG_008272.1:g.58663A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355773.6:c.1349A= MANE Select	ENSP00000348019.5:p.Asp450=
ENST00000355773.5:c.1349A=	ENSP00000348019.5:p.Asp450=
NM_012434.4:c.1349A=	NP_036566.1:p.Asp450=
XM_005248710.2:c.1298A=	XP_005248767.1:p.Asp433=
XM_005248711.1:c.1151A=	XP_005248768.1:p.Asp384=
XM_011535750.1:c.*7A=	XP_011534052.1:n.*7A=
NM_012434.5:c.1349A= MANE Select	NP_036566.1:p.Asp450=
NM_001382629.1:c.1118A=	NP_001369558.1:p.Asp373=
NM_001382630.1:c.1260-5138A=	NP_001369559.1:n.1260-5138A=
NM_001382631.1:c.1370A=	NP_001369560.1:p.Asp457=
NM_001382632.1:c.1262A=	NP_001369561.1:p.Asp421=
NM_001382633.1:c.1349A=	NP_001369562.1:p.Asp450=
NM_001382634.1:c.1190A=	NP_001369563.1:p.Asp397=
NM_001382635.1:c.1346A=	NP_001369564.1:p.Asp449=
NM_001382636.1:c.1031A=	NP_001369565.1:p.Asp344=