Canonical Allele Identifier: CA1638223415

Gene: SLC17A5

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73642067_73642071delinsGGTGA , CM000668.2:g.73642067_73642071delinsGGTGA	GRCh38
NC_000006.11:g.74351790_74351794delinsGGTGA , CM000668.1:g.74351790_74351794delinsGGTGA	GRCh37
NC_000006.10:g.74408511_74408515delinsGGTGA	NCBI36
NG_008272.1:g.16944_16948delinsTCACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355773.6:c.292-147_292-143delinsTCACC MANE Select	ENSP00000348019.5:n.292-147_292-143delinsTCACC
ENST00000355773.5:c.292-147_292-143delinsTCACC	ENSP00000348019.5:n.292-147_292-143delinsTCACC
ENST00000481996.1:n.58-147_58-143delinsTCACC
NM_012434.4:c.292-147_292-143delinsTCACC	NP_036566.1:n.292-147_292-143delinsTCACC
XM_005248710.2:c.241-147_241-143delinsTCACC	XP_005248767.1:n.241-147_241-143delinsTCACC
XM_005248711.1:c.94-147_94-143delinsTCACC	XP_005248768.1:n.94-147_94-143delinsTCACC
XM_011535750.1:c.292-147_292-143delinsTCACC	XP_011534052.1:n.292-147_292-143delinsTCACC
XM_011535751.1:c.292-147_292-143delinsTCACC	XP_011534053.1:n.292-147_292-143delinsTCACC
NM_012434.5:c.292-147_292-143delinsTCACC MANE Select	NP_036566.1:n.292-147_292-143delinsTCACC
NM_001382629.1:c.61-147_61-143delinsTCACC	NP_001369558.1:n.61-147_61-143delinsTCACC
NM_001382630.1:c.292-147_292-143delinsTCACC	NP_001369559.1:n.292-147_292-143delinsTCACC
NM_001382631.1:c.313-147_313-143delinsTCACC	NP_001369560.1:n.313-147_313-143delinsTCACC
NM_001382632.1:c.292-147_292-143delinsTCACC	NP_001369561.1:n.292-147_292-143delinsTCACC
NM_001382633.1:c.292-147_292-143delinsTCACC	NP_001369562.1:n.292-147_292-143delinsTCACC
NM_001382634.1:c.292-147_292-143delinsTCACC	NP_001369563.1:n.292-147_292-143delinsTCACC
NM_001382635.1:c.292-147_292-143delinsTCACC	NP_001369564.1:n.292-147_292-143delinsTCACC
NM_001382636.1:c.61-147_61-143delinsTCACC	NP_001369565.1:n.61-147_61-143delinsTCACC