Canonical Allele Identifier: CA9358870

Gene: SLC7A9

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.32864249C>T , CM000681.2:g.32864249C>T	GRCh38
NC_000019.9:g.33355155C>T , CM000681.1:g.33355155C>T	GRCh37
NC_000019.8:g.38046995C>T	NCBI36
NG_008258.1:g.10529G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_014270.5:c.325G>A MANE Select	NP_055085.1:p.Ala109Thr
ENST00000023064.9:c.325G>A MANE Select	ENSP00000023064.3:p.Ala109Thr
NM_001126335.1:c.325G>A	NP_001119807.1:p.Ala109Thr
NM_001126335.2:c.325G>A	NP_001119807.1:p.Ala109Thr
NM_001243036.1:c.325G>A	NP_001229965.1:p.Ala109Thr
NM_001243036.2:c.325G>A	NP_001229965.1:p.Ala109Thr
NM_014270.4:c.325G>A	NP_055085.1:p.Ala109Thr
ENST00000023064.8:c.325G>A	ENSP00000023064.3:p.Ala109Thr
ENST00000587772.1:c.325G>A	ENSP00000468439.1:p.Ala109Thr
ENST00000589659.1:n.270G>A
ENST00000590341.5:c.325G>A	ENSP00000464822.1:p.Ala109Thr
ENST00000590465.5:c.*57G>A	ENSP00000468076.1:n.*57G>A
ENST00000592232.5:c.*57G>A	ENSP00000465563.1:n.*57G>A
XM_006722992.1:c.-131G>A	XP_006723055.1:n.-131G>A
XM_011526402.1:c.325G>A	XP_011524704.1:p.Ala109Thr
XM_011526402.3:c.325G>A	XP_011524704.1:p.Ala109Thr
XM_017026230.1:c.61G>A	XP_016881719.1:p.Ala21Thr
XM_024451334.1:c.-718G>A	XP_024307102.1:n.-718G>A