Canonical Allele Identifier: CA450912390

Gene: SLC17A5

Linked Data

• MyVariant Identifiers: chr6:g.74354235A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73644512A>T , CM000668.2:g.73644512A>T	GRCh38
NC_000006.11:g.74354235A>T , CM000668.1:g.74354235A>T	GRCh37
NC_000006.10:g.74410956A>T	NCBI36
NG_008272.1:g.14503T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000355773.6:c.186T>A MANE Select	ENSP00000348019.5:p.Val62=
ENST00000355773.5:c.186T>A	ENSP00000348019.5:p.Val62=
NM_012434.4:c.186T>A	NP_036566.1:p.Val62=
XM_005248710.2:c.135T>A	XP_005248767.1:p.Val45=
XM_005248711.1:c.-13T>A	XP_005248768.1:n.-13T>A
XM_011535750.1:c.186T>A	XP_011534052.1:p.Val62=
XM_011535751.1:c.186T>A	XP_011534053.1:p.Val62=
NM_012434.5:c.186T>A MANE Select	NP_036566.1:p.Val62=
NM_001382629.1:c.61-2588T>A	NP_001369558.1:n.61-2588T>A
NM_001382630.1:c.186T>A	NP_001369559.1:p.Val62=
NM_001382631.1:c.207T>A	NP_001369560.1:p.Val69=
NM_001382632.1:c.186T>A	NP_001369561.1:p.Val62=
NM_001382633.1:c.186T>A	NP_001369562.1:p.Val62=
NM_001382634.1:c.186T>A	NP_001369563.1:p.Val62=
NM_001382635.1:c.186T>A	NP_001369564.1:p.Val62=
NM_001382636.1:c.61-2588T>A	NP_001369565.1:n.61-2588T>A