Canonical Allele Identifier: CA14744374

Gene: SLC7A9

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.32868885A>T , CM000681.2:g.32868885A>T	GRCh38
NC_000019.9:g.33359791A>T , CM000681.1:g.33359791A>T	GRCh37
NC_000019.8:g.38051631A>T	NCBI36
NG_008258.1:g.5893T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_014270.5:c.-111-240T>A MANE Select	NP_055085.1:n.-111-240T>A
ENST00000023064.9:c.-111-240T>A MANE Select	ENSP00000023064.3:n.-111-240T>A
NM_001126335.1:c.-25-326T>A	NP_001119807.1:n.-25-326T>A
NM_001126335.2:c.-25-326T>A	NP_001119807.1:n.-25-326T>A
NM_001243036.1:c.-111-240T>A	NP_001229965.1:n.-111-240T>A
NM_001243036.2:c.-111-240T>A	NP_001229965.1:n.-111-240T>A
NM_014270.4:c.-111-240T>A	NP_055085.1:n.-111-240T>A
ENST00000023064.8:c.-111-240T>A	ENSP00000023064.3:n.-111-240T>A
ENST00000587772.1:c.-25-326T>A	ENSP00000468439.1:n.-25-326T>A
ENST00000590341.5:c.-111-240T>A	ENSP00000464822.1:n.-111-240T>A
ENST00000590465.5:c.-111-240T>A	ENSP00000468076.1:n.-111-240T>A
XM_006722992.1:c.-480-326T>A	XP_006723055.1:n.-480-326T>A
XM_011526402.1:c.-25-326T>A	XP_011524704.1:n.-25-326T>A
XM_011526402.3:c.-25-326T>A	XP_011524704.1:n.-25-326T>A