Canonical Allele Identifier: CA1616765521

Gene: SLC17A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.25812694_25812698delinsCAGTT , CM000668.2:g.25812694_25812698delinsCAGTT	GRCh38
NC_000006.11:g.25812922_25812926delinsCAGTT , CM000668.1:g.25812922_25812926delinsCAGTT	GRCh37
NC_000006.10:g.25920901_25920905delinsCAGTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244527.10:c.897+133_897+137delinsAACTG MANE Select	ENSP00000244527.4:n.897+133_897+137delinsAACTG
ENST00000244527.8:c.897+133_897+137delinsAACTG	ENSP00000244527.4:n.897+133_897+137delinsAACTG
ENST00000377886.6:c.*148+133_*148+137delinsAACTG	ENSP00000367118.2:n.*148+133_*148+137delinsAACTG
ENST00000468082.1:c.735+397_735+401delinsAACTG	ENSP00000420546.1:n.735+397_735+401delinsAACTG
ENST00000476801.5:c.897+133_897+137delinsAACTG	ENSP00000420614.1:n.897+133_897+137delinsAACTG
NM_005074.3:c.897+133_897+137delinsAACTG	NP_005065.2:n.897+133_897+137delinsAACTG
XM_011514818.1:c.897+133_897+137delinsAACTG	XP_011513120.1:n.897+133_897+137delinsAACTG
XM_011514819.1:c.810+133_810+137delinsAACTG	XP_011513121.1:n.810+133_810+137delinsAACTG
XM_011514820.1:c.735+397_735+401delinsAACTG	XP_011513122.1:n.735+397_735+401delinsAACTG
XM_011514821.1:c.684+133_684+137delinsAACTG	XP_011513123.1:n.684+133_684+137delinsAACTG
XM_011514818.2:c.1047+133_1047+137delinsAACTG	XP_011513120.2:n.1047+133_1047+137delinsAACTG
XM_011514819.2:c.960+133_960+137delinsAACTG	XP_011513121.2:n.960+133_960+137delinsAACTG
XM_011514820.2:c.885+397_885+401delinsAACTG	XP_011513122.2:n.885+397_885+401delinsAACTG
XM_011514821.2:c.684+133_684+137delinsAACTG	XP_011513123.1:n.684+133_684+137delinsAACTG
XM_017011199.1:c.1047+133_1047+137delinsAACTG	XP_016866688.1:n.1047+133_1047+137delinsAACTG
XM_017011200.1:c.1047+133_1047+137delinsAACTG	XP_016866689.1:n.1047+133_1047+137delinsAACTG
XM_017011201.2:c.1047+133_1047+137delinsAACTG	XP_016866690.1:n.1047+133_1047+137delinsAACTG
XM_017011202.1:c.963+133_963+137delinsAACTG	XP_016866691.1:n.963+133_963+137delinsAACTG
NM_005074.5:c.897+133_897+137delinsAACTG MANE Select	NP_005065.2:n.897+133_897+137delinsAACTG