Canonical Allele Identifier: CA650449479

Gene: SLC17A5

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73641946_73641947insG , CM000668.2:g.73641946_73641947insG	GRCh38
NC_000006.11:g.74351669_74351670insG , CM000668.1:g.74351669_74351670insG	GRCh37
NC_000006.10:g.74408390_74408391insG	NCBI36
NG_008272.1:g.17068_17069insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355773.6:c.292-23_292-22insC MANE Select	ENSP00000348019.5:n.292-23_292-22insC
ENST00000355773.5:c.292-23_292-22insC	ENSP00000348019.5:n.292-23_292-22insC
ENST00000481996.1:n.58-23_58-22insC
NM_012434.4:c.292-23_292-22insC	NP_036566.1:n.292-23_292-22insC
XM_005248710.2:c.241-23_241-22insC	XP_005248767.1:n.241-23_241-22insC
XM_005248711.1:c.94-23_94-22insC	XP_005248768.1:n.94-23_94-22insC
XM_011535750.1:c.292-23_292-22insC	XP_011534052.1:n.292-23_292-22insC
XM_011535751.1:c.292-23_292-22insC	XP_011534053.1:n.292-23_292-22insC
NM_012434.5:c.292-23_292-22insC MANE Select	NP_036566.1:n.292-23_292-22insC
NM_001382629.1:c.61-23_61-22insC	NP_001369558.1:n.61-23_61-22insC
NM_001382630.1:c.292-23_292-22insC	NP_001369559.1:n.292-23_292-22insC
NM_001382631.1:c.313-23_313-22insC	NP_001369560.1:n.313-23_313-22insC
NM_001382632.1:c.292-23_292-22insC	NP_001369561.1:n.292-23_292-22insC
NM_001382633.1:c.292-23_292-22insC	NP_001369562.1:n.292-23_292-22insC
NM_001382634.1:c.292-23_292-22insC	NP_001369563.1:n.292-23_292-22insC
NM_001382635.1:c.292-23_292-22insC	NP_001369564.1:n.292-23_292-22insC
NM_001382636.1:c.61-23_61-22insC	NP_001369565.1:n.61-23_61-22insC