Canonical Allele Identifier: CA1638223079

Gene: SLC17A5

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73641810T= , CM000668.2:g.73641810T=	GRCh38
NC_000006.11:g.74351533T= , CM000668.1:g.74351533T=	GRCh37
NC_000006.10:g.74408254T=	NCBI36
NG_008272.1:g.17205A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355773.6:c.406A= MANE Select	ENSP00000348019.5:p.Lys136=
ENST00000355773.5:c.406A=	ENSP00000348019.5:p.Lys136=
ENST00000481996.1:n.172A=
NM_012434.4:c.406A=	NP_036566.1:p.Lys136=
XM_005248710.2:c.355A=	XP_005248767.1:p.Lys119=
XM_005248711.1:c.208A=	XP_005248768.1:p.Lys70=
XM_011535750.1:c.406A=	XP_011534052.1:p.Lys136=
XM_011535751.1:c.406A=	XP_011534053.1:p.Lys136=
NM_012434.5:c.406A= MANE Select	NP_036566.1:p.Lys136=
NM_001382629.1:c.175A=	NP_001369558.1:p.Lys59=
NM_001382630.1:c.406A=	NP_001369559.1:p.Lys136=
NM_001382631.1:c.427A=	NP_001369560.1:p.Lys143=
NM_001382632.1:c.406A=	NP_001369561.1:p.Lys136=
NM_001382633.1:c.406A=	NP_001369562.1:p.Lys136=
NM_001382634.1:c.406A=	NP_001369563.1:p.Lys136=
NM_001382635.1:c.406A=	NP_001369564.1:p.Lys136=
NM_001382636.1:c.175A=	NP_001369565.1:p.Lys59=