Canonical Allele Identifier: CA1638234802

Gene: SLC17A5

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73621903A= , CM000668.2:g.73621903A=	GRCh38
NC_000006.11:g.74331626A= , CM000668.1:g.74331626A=	GRCh37
NC_000006.10:g.74388347A=	NCBI36
NG_008272.1:g.37112T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000355773.6:c.879T= MANE Select	ENSP00000348019.5:p.Ala293=
ENST00000355773.5:c.879T=	ENSP00000348019.5:p.Ala293=
NM_012434.4:c.879T=	NP_036566.1:p.Ala293=
XM_005248710.2:c.828T=	XP_005248767.1:p.Ala276=
XM_005248711.1:c.681T=	XP_005248768.1:p.Ala227=
XM_011535750.1:c.879T=	XP_011534052.1:p.Ala293=
NM_012434.5:c.879T= MANE Select	NP_036566.1:p.Ala293=
NM_001382629.1:c.648T=	NP_001369558.1:p.Ala216=
NM_001382630.1:c.879T=	NP_001369559.1:p.Ala293=
NM_001382631.1:c.900T=	NP_001369560.1:p.Ala300=
NM_001382632.1:c.792T=	NP_001369561.1:p.Ala264=
NM_001382633.1:c.879T=	NP_001369562.1:p.Ala293=
NM_001382634.1:c.820-6456T=	NP_001369563.1:n.820-6456T=
NM_001382635.1:c.876T=	NP_001369564.1:p.Ala292=
NM_001382636.1:c.561T=	NP_001369565.1:p.Ala187=