Canonical Allele Identifier: CA1638231823

Gene: SLC17A5

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73615410C= , CM000668.2:g.73615410C=	GRCh38
NC_000006.11:g.74325133C= , CM000668.1:g.74325133C=	GRCh37
NC_000006.10:g.74381854C=	NCBI36
NG_008272.1:g.43605G=

Transcript Alleles

HGVS	Amino-acid Change
NM_012434.5:c.1016G= MANE Select	NP_036566.1:p.Trp339=
ENST00000355773.6:c.1016G= MANE Select	ENSP00000348019.5:p.Trp339=
NM_001382629.1:c.785G=	NP_001369558.1:p.Trp262=
NM_001382630.1:c.1016G=	NP_001369559.1:p.Trp339=
NM_001382631.1:c.1037G=	NP_001369560.1:p.Trp346=
NM_001382632.1:c.929G=	NP_001369561.1:p.Trp310=
NM_001382633.1:c.1016G=	NP_001369562.1:p.Trp339=
NM_001382634.1:c.857G=	NP_001369563.1:p.Trp286=
NM_001382635.1:c.1013G=	NP_001369564.1:p.Trp338=
NM_001382636.1:c.698G=	NP_001369565.1:p.Trp233=
NM_012434.4:c.1016G=	NP_036566.1:p.Trp339=
ENST00000355773.5:c.1016G=	ENSP00000348019.5:p.Trp339=
XM_005248710.2:c.965G=	XP_005248767.1:p.Trp322=
XM_005248711.1:c.818G=	XP_005248768.1:p.Trp273=
XM_011535750.1:c.1016G=	XP_011534052.1:p.Trp339=