Canonical Allele Identifier: CA1638234787

Gene: SLC17A5

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73621873C= , CM000668.2:g.73621873C=	GRCh38
NC_000006.11:g.74331596C= , CM000668.1:g.74331596C=	GRCh37
NC_000006.10:g.74388317C=	NCBI36
NG_008272.1:g.37142G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355773.6:c.909G= MANE Select	ENSP00000348019.5:p.Trp303=
ENST00000355773.5:c.909G=	ENSP00000348019.5:p.Trp303=
NM_012434.4:c.909G=	NP_036566.1:p.Trp303=
XM_005248710.2:c.858G=	XP_005248767.1:p.Trp286=
XM_005248711.1:c.711G=	XP_005248768.1:p.Trp237=
XM_011535750.1:c.909G=	XP_011534052.1:p.Trp303=
NM_012434.5:c.909G= MANE Select	NP_036566.1:p.Trp303=
NM_001382629.1:c.678G=	NP_001369558.1:p.Trp226=
NM_001382630.1:c.909G=	NP_001369559.1:p.Trp303=
NM_001382631.1:c.930G=	NP_001369560.1:p.Trp310=
NM_001382632.1:c.822G=	NP_001369561.1:p.Trp274=
NM_001382633.1:c.909G=	NP_001369562.1:p.Trp303=
NM_001382634.1:c.820-6426G=	NP_001369563.1:n.820-6426G=
NM_001382635.1:c.906G=	NP_001369564.1:p.Trp302=
NM_001382636.1:c.591G=	NP_001369565.1:p.Trp197=