Canonical Allele Identifier: CA1638223050

Gene: SLC17A5

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73641795A= , CM000668.2:g.73641795A=	GRCh38
NC_000006.11:g.74351518A= , CM000668.1:g.74351518A=	GRCh37
NC_000006.10:g.74408239A=	NCBI36
NG_008272.1:g.17220T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000355773.6:c.421T= MANE Select	ENSP00000348019.5:p.Phe141=
ENST00000355773.5:c.421T=	ENSP00000348019.5:p.Phe141=
ENST00000481996.1:n.187T=
NM_012434.4:c.421T=	NP_036566.1:p.Phe141=
XM_005248710.2:c.370T=	XP_005248767.1:p.Phe124=
XM_005248711.1:c.223T=	XP_005248768.1:p.Phe75=
XM_011535750.1:c.421T=	XP_011534052.1:p.Phe141=
XM_011535751.1:c.421T=	XP_011534053.1:p.Phe141=
NM_012434.5:c.421T= MANE Select	NP_036566.1:p.Phe141=
NM_001382629.1:c.190T=	NP_001369558.1:p.Phe64=
NM_001382630.1:c.421T=	NP_001369559.1:p.Phe141=
NM_001382631.1:c.442T=	NP_001369560.1:p.Phe148=
NM_001382632.1:c.421T=	NP_001369561.1:p.Phe141=
NM_001382633.1:c.421T=	NP_001369562.1:p.Phe141=
NM_001382634.1:c.421T=	NP_001369563.1:p.Phe141=
NM_001382635.1:c.421T=	NP_001369564.1:p.Phe141=
NM_001382636.1:c.190T=	NP_001369565.1:p.Phe64=