Canonical Allele Identifier: CA363157834

Gene: SLC17A1

Linked Data

• MyVariant Identifiers: chr6:g.25813088T>G (hg19) ; chr6:g.25812860T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.25812860T>G , CM000668.2:g.25812860T>G	GRCh38
NC_000006.11:g.25813088T>G , CM000668.1:g.25813088T>G	GRCh37
NC_000006.10:g.25921067T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244527.10:c.868A>C MANE Select	ENSP00000244527.4:p.Asn290His
ENST00000244527.8:c.868A>C	ENSP00000244527.4:p.Asn290His
ENST00000377886.6:c.*119A>C	ENSP00000367118.2:n.*119A>C
ENST00000468082.1:c.735+235A>C	ENSP00000420546.1:n.735+235A>C
ENST00000476801.5:c.868A>C	ENSP00000420614.1:p.Asn290His
NM_005074.3:c.868A>C	NP_005065.2:p.Asn290His
XM_011514818.1:c.868A>C	XP_011513120.1:p.Asn290His
XM_011514819.1:c.781A>C	XP_011513121.1:p.Asn261His
XM_011514820.1:c.735+235A>C	XP_011513122.1:n.735+235A>C
XM_011514821.1:c.655A>C	XP_011513123.1:p.Asn219His
XM_011514818.2:c.1018A>C	XP_011513120.2:p.Asn340His
XM_011514819.2:c.931A>C	XP_011513121.2:p.Asn311His
XM_011514820.2:c.885+235A>C	XP_011513122.2:n.885+235A>C
XM_011514821.2:c.655A>C	XP_011513123.1:p.Asn219His
XM_017011199.1:c.1018A>C	XP_016866688.1:p.Asn340His
XM_017011200.1:c.1018A>C	XP_016866689.1:p.Asn340His
XM_017011201.2:c.1018A>C	XP_016866690.1:p.Asn340His
XM_017011202.1:c.934A>C	XP_016866691.1:p.Asn312His
NM_005074.5:c.868A>C MANE Select	NP_005065.2:p.Asn290His