Canonical Allele Identifier: CA307504393

Gene: SLC7A9

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.32858800_32858803dup , CM000681.2:g.32858800_32858803dup	GRCh38
NC_000019.9:g.33349706_33349709dup , CM000681.1:g.33349706_33349709dup	GRCh37
NC_000019.8:g.38041546_38041549dup	NCBI36
NG_008258.1:g.16006_16009dup

Transcript Alleles

HGVS	Amino-acid Change
NM_014270.5:c.874-229_874-226dup MANE Select	NP_055085.1:n.874-229_874-226dup
ENST00000023064.9:c.874-229_874-226dup MANE Select	ENSP00000023064.3:n.874-229_874-226dup
NM_001126335.1:c.874-229_874-226dup	NP_001119807.1:n.874-229_874-226dup
NM_001126335.2:c.874-229_874-226dup	NP_001119807.1:n.874-229_874-226dup
NM_001243036.1:c.874-229_874-226dup	NP_001229965.1:n.874-229_874-226dup
NM_001243036.2:c.874-229_874-226dup	NP_001229965.1:n.874-229_874-226dup
NM_014270.4:c.874-229_874-226dup	NP_055085.1:n.874-229_874-226dup
ENST00000023064.8:c.874-229_874-226dup	ENSP00000023064.3:n.874-229_874-226dup
ENST00000587772.1:c.874-229_874-226dup	ENSP00000468439.1:n.874-229_874-226dup
ENST00000589659.1:n.819-229_819-226dup
ENST00000590341.5:c.874-229_874-226dup	ENSP00000464822.1:n.874-229_874-226dup
ENST00000590465.5:c.*1021-229_*1021-226dup	ENSP00000468076.1:n.*1021-229_*1021-226dup
ENST00000592232.5:c.*380-229_*380-226dup	ENSP00000465563.1:n.*380-229_*380-226dup
XM_006722992.1:c.193-229_193-226dup	XP_006723055.1:n.193-229_193-226dup
XM_011526402.1:c.874-229_874-226dup	XP_011524704.1:n.874-229_874-226dup
XM_011526402.3:c.874-229_874-226dup	XP_011524704.1:n.874-229_874-226dup
XM_017026230.1:c.610-229_610-226dup	XP_016881719.1:n.610-229_610-226dup
XM_024451334.1:c.247-229_247-226dup	XP_024307102.1:n.247-229_247-226dup