Canonical Allele Identifier: CA1638223881

Gene: SLC17A5

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73600394G= , CM000668.2:g.73600394G=	GRCh38
NC_000006.11:g.74310117G= , CM000668.1:g.74310117G=	GRCh37
NC_000006.10:g.74366838G=	NCBI36
NG_008272.1:g.58621C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355773.6:c.1307C= MANE Select	ENSP00000348019.5:p.Pro436=
ENST00000355773.5:c.1307C=	ENSP00000348019.5:p.Pro436=
NM_012434.4:c.1307C=	NP_036566.1:p.Pro436=
XM_005248710.2:c.1256C=	XP_005248767.1:p.Pro419=
XM_005248711.1:c.1109C=	XP_005248768.1:p.Pro370=
XM_011535750.1:c.1159C=	XP_011534052.1:p.Gln387=
NM_012434.5:c.1307C= MANE Select	NP_036566.1:p.Pro436=
NM_001382629.1:c.1076C=	NP_001369558.1:p.Pro359=
NM_001382630.1:c.1260-5180C=	NP_001369559.1:n.1260-5180C=
NM_001382631.1:c.1328C=	NP_001369560.1:p.Pro443=
NM_001382632.1:c.1220C=	NP_001369561.1:p.Pro407=
NM_001382633.1:c.1307C=	NP_001369562.1:p.Pro436=
NM_001382634.1:c.1148C=	NP_001369563.1:p.Pro383=
NM_001382635.1:c.1304C=	NP_001369564.1:p.Pro435=
NM_001382636.1:c.989C=	NP_001369565.1:p.Pro330=