Canonical Allele Identifier: CA1638229749

Gene: SLC17A5

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73610433C= , CM000668.2:g.73610433C=	GRCh38
NC_000006.11:g.74320156C= , CM000668.1:g.74320156C=	GRCh37
NC_000006.10:g.74376877C=	NCBI36
NG_008272.1:g.48582G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355773.6:c.1226G= MANE Select	ENSP00000348019.5:p.Gly409=
ENST00000355773.5:c.1226G=	ENSP00000348019.5:p.Gly409=
NM_012434.4:c.1226G=	NP_036566.1:p.Gly409=
XM_005248710.2:c.1175G=	XP_005248767.1:p.Gly392=
XM_005248711.1:c.1028G=	XP_005248768.1:p.Gly343=
XM_011535750.1:c.1111+4882G=	XP_011534052.1:n.1111+4882G=
NM_012434.5:c.1226G= MANE Select	NP_036566.1:p.Gly409=
NM_001382629.1:c.995G=	NP_001369558.1:p.Gly332=
NM_001382630.1:c.1226G=	NP_001369559.1:p.Gly409=
NM_001382631.1:c.1247G=	NP_001369560.1:p.Gly416=
NM_001382632.1:c.1139G=	NP_001369561.1:p.Gly380=
NM_001382633.1:c.1226G=	NP_001369562.1:p.Gly409=
NM_001382634.1:c.1067G=	NP_001369563.1:p.Gly356=
NM_001382635.1:c.1223G=	NP_001369564.1:p.Gly408=
NM_001382636.1:c.908G=	NP_001369565.1:p.Gly303=