Canonical Allele Identifier: CA2332455415

Gene: SLC7A9

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.32862146A= , CM000681.2:g.32862146A=	GRCh38
NC_000019.9:g.33353052A= , CM000681.1:g.33353052A=	GRCh37
NC_000019.8:g.38044892A=	NCBI36
NG_008258.1:g.12632T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000023064.9:c.676T= MANE Select	ENSP00000023064.3:p.Tyr226=
ENST00000023064.8:c.676T=	ENSP00000023064.3:p.Tyr226=
ENST00000587772.1:c.676T=	ENSP00000468439.1:p.Tyr226=
ENST00000589659.1:n.621T=
ENST00000590341.5:c.676T=	ENSP00000464822.1:p.Tyr226=
ENST00000590465.5:c.*211-1496T=	ENSP00000468076.1:n.*211-1496T=
ENST00000592232.5:c.*211-1496T=	ENSP00000465563.1:n.*211-1496T=
NM_001126335.1:c.676T=	NP_001119807.1:p.Tyr226=
NM_001243036.1:c.676T=	NP_001229965.1:p.Tyr226=
NM_014270.4:c.676T=	NP_055085.1:p.Tyr226=
XM_006722992.1:c.24-1496T=	XP_006723055.1:n.24-1496T=
XM_011526402.1:c.676T=	XP_011524704.1:p.Tyr226=
XM_011526402.3:c.676T=	XP_011524704.1:p.Tyr226=
XM_017026230.1:c.412T=	XP_016881719.1:p.Tyr138=
XM_024451334.1:c.-564-1496T=	XP_024307102.1:n.-564-1496T=
NM_014270.5:c.676T= MANE Select	NP_055085.1:p.Tyr226=
NM_001126335.2:c.676T=	NP_001119807.1:p.Tyr226=
NM_001243036.2:c.676T=	NP_001229965.1:p.Tyr226=