Canonical Allele Identifier: CA2332455421

Gene: SLC7A9

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.32862163G= , CM000681.2:g.32862163G=	GRCh38
NC_000019.9:g.33353069G= , CM000681.1:g.33353069G=	GRCh37
NC_000019.8:g.38044909G=	NCBI36
NG_008258.1:g.12615C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000023064.9:c.659C= MANE Select	ENSP00000023064.3:p.Ala220=
ENST00000023064.8:c.659C=	ENSP00000023064.3:p.Ala220=
ENST00000587772.1:c.659C=	ENSP00000468439.1:p.Ala220=
ENST00000589659.1:n.604C=
ENST00000590341.5:c.659C=	ENSP00000464822.1:p.Ala220=
ENST00000590465.5:c.*211-1513C=	ENSP00000468076.1:n.*211-1513C=
ENST00000592232.5:c.*211-1513C=	ENSP00000465563.1:n.*211-1513C=
NM_001126335.1:c.659C=	NP_001119807.1:p.Ala220=
NM_001243036.1:c.659C=	NP_001229965.1:p.Ala220=
NM_014270.4:c.659C=	NP_055085.1:p.Ala220=
XM_006722992.1:c.24-1513C=	XP_006723055.1:n.24-1513C=
XM_011526402.1:c.659C=	XP_011524704.1:p.Ala220=
XM_011526402.3:c.659C=	XP_011524704.1:p.Ala220=
XM_017026230.1:c.395C=	XP_016881719.1:p.Ala132=
XM_024451334.1:c.-564-1513C=	XP_024307102.1:n.-564-1513C=
NM_014270.5:c.659C= MANE Select	NP_055085.1:p.Ala220=
NM_001126335.2:c.659C=	NP_001119807.1:p.Ala220=
NM_001243036.2:c.659C=	NP_001229965.1:p.Ala220=