Canonical Allele Identifier: CA10627566

Gene: SLC17A5

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73594517C>T , CM000668.2:g.73594517C>T	GRCh38
NC_000006.11:g.74304240C>T , CM000668.1:g.74304240C>T	GRCh37
NC_000006.10:g.74360961C>T	NCBI36
NG_008272.1:g.64498G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355773.6:c.*560G>A MANE Select	ENSP00000348019.5:n.*560G>A
ENST00000355773.5:c.*560G>A	ENSP00000348019.5:n.*560G>A
NM_012434.4:c.*560G>A	NP_036566.1:n.*560G>A
XM_005248710.2:c.*560G>A	XP_005248767.1:n.*560G>A
XM_005248711.1:c.*560G>A	XP_005248768.1:n.*560G>A
XM_011535750.1:c.*706G>A	XP_011534052.1:n.*706G>A
NM_012434.5:c.*560G>A MANE Select	NP_036566.1:n.*560G>A
NM_001382629.1:c.*560G>A	NP_001369558.1:n.*560G>A
NM_001382630.1:c.*544G>A	NP_001369559.1:n.*544G>A
NM_001382631.1:c.*560G>A	NP_001369560.1:n.*560G>A
NM_001382632.1:c.*560G>A	NP_001369561.1:n.*560G>A
NM_001382633.1:c.*544G>A	NP_001369562.1:n.*544G>A
NM_001382634.1:c.*560G>A	NP_001369563.1:n.*560G>A
NM_001382635.1:c.*560G>A	NP_001369564.1:n.*560G>A
NM_001382636.1:c.*560G>A	NP_001369565.1:n.*560G>A