Canonical Allele Identifier: CA1638225399

Gene: SLC17A5

Linked Data

• dbSNP Id: rs1769435722

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73644338_73644350del , CM000668.2:g.73644338_73644350del	GRCh38
NC_000006.11:g.74354061_74354073del , CM000668.1:g.74354061_74354073del	GRCh37
NC_000006.10:g.74410782_74410794del	NCBI36
NG_008272.1:g.14665_14677del

Transcript Alleles

HGVS	Amino-acid change
ENST00000355773.6:c.291+57_291+69del MANE Select	ENSP00000348019.5:n.291+57_291+69del
ENST00000355773.5:c.291+57_291+69del	ENSP00000348019.5:n.291+57_291+69del
ENST00000481996.1:n.57+57_57+69del
NM_012434.4:c.291+57_291+69del	NP_036566.1:n.291+57_291+69del
XM_005248710.2:c.240+57_240+69del	XP_005248767.1:n.240+57_240+69del
XM_005248711.1:c.93+57_93+69del	XP_005248768.1:n.93+57_93+69del
XM_011535750.1:c.291+57_291+69del	XP_011534052.1:n.291+57_291+69del
XM_011535751.1:c.291+57_291+69del	XP_011534053.1:n.291+57_291+69del
NM_012434.5:c.291+57_291+69del MANE Select	NP_036566.1:n.291+57_291+69del
NM_001382629.1:c.61-2426_61-2414del	NP_001369558.1:n.61-2426_61-2414del
NM_001382630.1:c.291+57_291+69del	NP_001369559.1:n.291+57_291+69del
NM_001382631.1:c.312+57_312+69del	NP_001369560.1:n.312+57_312+69del
NM_001382632.1:c.291+57_291+69del	NP_001369561.1:n.291+57_291+69del
NM_001382633.1:c.291+57_291+69del	NP_001369562.1:n.291+57_291+69del
NM_001382634.1:c.291+57_291+69del	NP_001369563.1:n.291+57_291+69del
NM_001382635.1:c.291+57_291+69del	NP_001369564.1:n.291+57_291+69del
NM_001382636.1:c.61-2426_61-2414del	NP_001369565.1:n.61-2426_61-2414del