Canonical Allele Identifier: CA1616765574

Gene: SLC17A1

Linked Data

• dbSNP Id: rs1764203310
• gnomAD v4: 6-25812785-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.25812788_25812789del , CM000668.2:g.25812788_25812789del	GRCh38
NC_000006.11:g.25813016_25813017del , CM000668.1:g.25813016_25813017del	GRCh37
NC_000006.10:g.25920995_25920996del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244527.10:c.897+44_897+45del MANE Select	ENSP00000244527.4:n.897+44_897+45del
ENST00000244527.8:c.897+44_897+45del	ENSP00000244527.4:n.897+44_897+45del
ENST00000377886.6:c.*148+44_*148+45del	ENSP00000367118.2:n.*148+44_*148+45del
ENST00000468082.1:c.735+308_735+309del	ENSP00000420546.1:n.735+308_735+309del
ENST00000476801.5:c.897+44_897+45del	ENSP00000420614.1:n.897+44_897+45del
NM_005074.3:c.897+44_897+45del	NP_005065.2:n.897+44_897+45del
XM_011514818.1:c.897+44_897+45del	XP_011513120.1:n.897+44_897+45del
XM_011514819.1:c.810+44_810+45del	XP_011513121.1:n.810+44_810+45del
XM_011514820.1:c.735+308_735+309del	XP_011513122.1:n.735+308_735+309del
XM_011514821.1:c.684+44_684+45del	XP_011513123.1:n.684+44_684+45del
XM_011514818.2:c.1047+44_1047+45del	XP_011513120.2:n.1047+44_1047+45del
XM_011514819.2:c.960+44_960+45del	XP_011513121.2:n.960+44_960+45del
XM_011514820.2:c.885+308_885+309del	XP_011513122.2:n.885+308_885+309del
XM_011514821.2:c.684+44_684+45del	XP_011513123.1:n.684+44_684+45del
XM_017011199.1:c.1047+44_1047+45del	XP_016866688.1:n.1047+44_1047+45del
XM_017011200.1:c.1047+44_1047+45del	XP_016866689.1:n.1047+44_1047+45del
XM_017011201.2:c.1047+44_1047+45del	XP_016866690.1:n.1047+44_1047+45del
XM_017011202.1:c.963+44_963+45del	XP_016866691.1:n.963+44_963+45del
NM_005074.5:c.897+44_897+45del MANE Select	NP_005065.2:n.897+44_897+45del