Canonical Allele Identifier: CA1638223822

Gene: SLC17A5

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73600368T= , CM000668.2:g.73600368T=	GRCh38
NC_000006.11:g.74310091T= , CM000668.1:g.74310091T=	GRCh37
NC_000006.10:g.74366812T=	NCBI36
NG_008272.1:g.58647A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355773.6:c.1333A= MANE Select	ENSP00000348019.5:p.Lys445=
ENST00000355773.5:c.1333A=	ENSP00000348019.5:p.Lys445=
NM_012434.4:c.1333A=	NP_036566.1:p.Lys445=
XM_005248710.2:c.1282A=	XP_005248767.1:p.Lys428=
XM_005248711.1:c.1135A=	XP_005248768.1:p.Lys379=
XM_011535750.1:c.1185A=	XP_011534052.1:p.Leu395=
NM_012434.5:c.1333A= MANE Select	NP_036566.1:p.Lys445=
NM_001382629.1:c.1102A=	NP_001369558.1:p.Lys368=
NM_001382630.1:c.1260-5154A=	NP_001369559.1:n.1260-5154A=
NM_001382631.1:c.1354A=	NP_001369560.1:p.Lys452=
NM_001382632.1:c.1246A=	NP_001369561.1:p.Lys416=
NM_001382633.1:c.1333A=	NP_001369562.1:p.Lys445=
NM_001382634.1:c.1174A=	NP_001369563.1:p.Lys392=
NM_001382635.1:c.1330A=	NP_001369564.1:p.Lys444=
NM_001382636.1:c.1015A=	NP_001369565.1:p.Lys339=