Canonical Allele Identifier: CA1638225553

Gene: SLC17A5

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73644482_73644483delinsTG , CM000668.2:g.73644482_73644483delinsTG	GRCh38
NC_000006.11:g.74354205_74354206delinsTG , CM000668.1:g.74354205_74354206delinsTG	GRCh37
NC_000006.10:g.74410926_74410927delinsTG	NCBI36
NG_008272.1:g.14532_14533delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000355773.6:c.215_216delinsCA MANE Select	ENSP00000348019.5:p.Thr72=
ENST00000355773.5:c.215_216delinsCA	ENSP00000348019.5:p.Thr72=
NM_012434.4:c.215_216delinsCA	NP_036566.1:p.Thr72=
XM_005248710.2:c.164_165delinsCA	XP_005248767.1:p.Thr55=
XM_005248711.1:c.17_18delinsCA	XP_005248768.1:p.Thr6=
XM_011535750.1:c.215_216delinsCA	XP_011534052.1:p.Thr72=
XM_011535751.1:c.215_216delinsCA	XP_011534053.1:p.Thr72=
NM_012434.5:c.215_216delinsCA MANE Select	NP_036566.1:p.Thr72=
NM_001382629.1:c.61-2559_61-2558delinsCA	NP_001369558.1:n.61-2559_61-2558delinsCA
NM_001382630.1:c.215_216delinsCA	NP_001369559.1:p.Thr72=
NM_001382631.1:c.236_237delinsCA	NP_001369560.1:p.Thr79=
NM_001382632.1:c.215_216delinsCA	NP_001369561.1:p.Thr72=
NM_001382633.1:c.215_216delinsCA	NP_001369562.1:p.Thr72=
NM_001382634.1:c.215_216delinsCA	NP_001369563.1:p.Thr72=
NM_001382635.1:c.215_216delinsCA	NP_001369564.1:p.Thr72=
NM_001382636.1:c.61-2559_61-2558delinsCA	NP_001369565.1:n.61-2559_61-2558delinsCA