Canonical Allele Identifier: CA1638234794

Gene: SLC17A5

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73621888G= , CM000668.2:g.73621888G=	GRCh38
NC_000006.11:g.74331611G= , CM000668.1:g.74331611G=	GRCh37
NC_000006.10:g.74388332G=	NCBI36
NG_008272.1:g.37127C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000355773.6:c.894C= MANE Select	ENSP00000348019.5:p.His298=
ENST00000355773.5:c.894C=	ENSP00000348019.5:p.His298=
NM_012434.4:c.894C=	NP_036566.1:p.His298=
XM_005248710.2:c.843C=	XP_005248767.1:p.His281=
XM_005248711.1:c.696C=	XP_005248768.1:p.His232=
XM_011535750.1:c.894C=	XP_011534052.1:p.His298=
NM_012434.5:c.894C= MANE Select	NP_036566.1:p.His298=
NM_001382629.1:c.663C=	NP_001369558.1:p.His221=
NM_001382630.1:c.894C=	NP_001369559.1:p.His298=
NM_001382631.1:c.915C=	NP_001369560.1:p.His305=
NM_001382632.1:c.807C=	NP_001369561.1:p.His269=
NM_001382633.1:c.894C=	NP_001369562.1:p.His298=
NM_001382634.1:c.820-6441C=	NP_001369563.1:n.820-6441C=
NM_001382635.1:c.891C=	NP_001369564.1:p.His297=
NM_001382636.1:c.576C=	NP_001369565.1:p.His192=