Canonical Allele Identifier: CA1638225468

Gene: SLC17A5

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73644424C= , CM000668.2:g.73644424C=	GRCh38
NC_000006.11:g.74354147C= , CM000668.1:g.74354147C=	GRCh37
NC_000006.10:g.74410868C=	NCBI36
NG_008272.1:g.14591G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355773.6:c.274G= MANE Select	ENSP00000348019.5:p.Val92=
ENST00000355773.5:c.274G=	ENSP00000348019.5:p.Val92=
ENST00000481996.1:n.40G=
NM_012434.4:c.274G=	NP_036566.1:p.Val92=
XM_005248710.2:c.223G=	XP_005248767.1:p.Val75=
XM_005248711.1:c.76G=	XP_005248768.1:p.Val26=
XM_011535750.1:c.274G=	XP_011534052.1:p.Val92=
XM_011535751.1:c.274G=	XP_011534053.1:p.Val92=
NM_012434.5:c.274G= MANE Select	NP_036566.1:p.Val92=
NM_001382629.1:c.61-2500G=	NP_001369558.1:n.61-2500G=
NM_001382630.1:c.274G=	NP_001369559.1:p.Val92=
NM_001382631.1:c.295G=	NP_001369560.1:p.Val99=
NM_001382632.1:c.274G=	NP_001369561.1:p.Val92=
NM_001382633.1:c.274G=	NP_001369562.1:p.Val92=
NM_001382634.1:c.274G=	NP_001369563.1:p.Val92=
NM_001382635.1:c.274G=	NP_001369564.1:p.Val92=
NM_001382636.1:c.61-2500G=	NP_001369565.1:n.61-2500G=