Canonical Allele Identifier: CA1638223007

Gene: SLC17A5

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73641758G= , CM000668.2:g.73641758G=	GRCh38
NC_000006.11:g.74351481G= , CM000668.1:g.74351481G=	GRCh37
NC_000006.10:g.74408202G=	NCBI36
NG_008272.1:g.17257C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355773.6:c.458C= MANE Select	ENSP00000348019.5:p.Thr153=
ENST00000355773.5:c.458C=	ENSP00000348019.5:p.Thr153=
ENST00000481996.1:n.224C=
NM_012434.4:c.458C=	NP_036566.1:p.Thr153=
XM_005248710.2:c.407C=	XP_005248767.1:p.Thr136=
XM_005248711.1:c.260C=	XP_005248768.1:p.Thr87=
XM_011535750.1:c.458C=	XP_011534052.1:p.Thr153=
XM_011535751.1:c.458C=	XP_011534053.1:p.Thr153=
NM_012434.5:c.458C= MANE Select	NP_036566.1:p.Thr153=
NM_001382629.1:c.227C=	NP_001369558.1:p.Thr76=
NM_001382630.1:c.458C=	NP_001369559.1:p.Thr153=
NM_001382631.1:c.479C=	NP_001369560.1:p.Thr160=
NM_001382632.1:c.458C=	NP_001369561.1:p.Thr153=
NM_001382633.1:c.458C=	NP_001369562.1:p.Thr153=
NM_001382634.1:c.458C=	NP_001369563.1:p.Thr153=
NM_001382635.1:c.458C=	NP_001369564.1:p.Thr153=
NM_001382636.1:c.227C=	NP_001369565.1:p.Thr76=