Canonical Allele Identifier: CA1638231834

Gene: SLC17A5

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73615443C= , CM000668.2:g.73615443C=	GRCh38
NC_000006.11:g.74325166C= , CM000668.1:g.74325166C=	GRCh37
NC_000006.10:g.74381887C=	NCBI36
NG_008272.1:g.43572G=

Transcript Alleles

HGVS	Amino-acid Change
NM_012434.5:c.983G= MANE Select	NP_036566.1:p.Gly328=
ENST00000355773.6:c.983G= MANE Select	ENSP00000348019.5:p.Gly328=
NM_001382629.1:c.752G=	NP_001369558.1:p.Gly251=
NM_001382630.1:c.983G=	NP_001369559.1:p.Gly328=
NM_001382631.1:c.1004G=	NP_001369560.1:p.Gly335=
NM_001382632.1:c.896G=	NP_001369561.1:p.Gly299=
NM_001382633.1:c.983G=	NP_001369562.1:p.Gly328=
NM_001382634.1:c.824G=	NP_001369563.1:p.Gly275=
NM_001382635.1:c.980G=	NP_001369564.1:p.Gly327=
NM_001382636.1:c.665G=	NP_001369565.1:p.Gly222=
NM_012434.4:c.983G=	NP_036566.1:p.Gly328=
ENST00000355773.5:c.983G=	ENSP00000348019.5:p.Gly328=
XM_005248710.2:c.932G=	XP_005248767.1:p.Gly311=
XM_005248711.1:c.785G=	XP_005248768.1:p.Gly262=
XM_011535750.1:c.983G=	XP_011534052.1:p.Gly328=