Canonical Allele Identifier: CA1638240632

Gene: SLC17A5

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73644596C= , CM000668.2:g.73644596C=	GRCh38
NC_000006.11:g.74354319C= , CM000668.1:g.74354319C=	GRCh37
NC_000006.10:g.74411040C=	NCBI36
NG_008272.1:g.14419G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355773.6:c.102G= MANE Select	ENSP00000348019.5:p.Val34=
ENST00000355773.5:c.102G=	ENSP00000348019.5:p.Val34=
NM_012434.4:c.102G=	NP_036566.1:p.Val34=
XM_005248710.2:c.51G=	XP_005248767.1:p.Val17=
XM_005248711.1:c.-97G=	XP_005248768.1:n.-97G=
XM_011535750.1:c.102G=	XP_011534052.1:p.Val34=
XM_011535751.1:c.102G=	XP_011534053.1:p.Val34=
NM_012434.5:c.102G= MANE Select	NP_036566.1:p.Val34=
NM_001382629.1:c.61-2672G=	NP_001369558.1:n.61-2672G=
NM_001382630.1:c.102G=	NP_001369559.1:p.Val34=
NM_001382631.1:c.123G=	NP_001369560.1:p.Val41=
NM_001382632.1:c.102G=	NP_001369561.1:p.Val34=
NM_001382633.1:c.102G=	NP_001369562.1:p.Val34=
NM_001382634.1:c.102G=	NP_001369563.1:p.Val34=
NM_001382635.1:c.102G=	NP_001369564.1:p.Val34=
NM_001382636.1:c.61-2672G=	NP_001369565.1:n.61-2672G=