Canonical Allele Identifier: CA405204345

Gene: SLC7A9

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.32864671A>G , CM000681.2:g.32864671A>G	GRCh38
NC_000019.9:g.33355577A>G , CM000681.1:g.33355577A>G	GRCh37
NC_000019.8:g.38047417A>G	NCBI36
NG_008258.1:g.10107T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_014270.5:c.193T>C MANE Select	NP_055085.1:p.Cys65Arg
ENST00000023064.9:c.193T>C MANE Select	ENSP00000023064.3:p.Cys65Arg
NM_001126335.1:c.193T>C	NP_001119807.1:p.Cys65Arg
NM_001126335.2:c.193T>C	NP_001119807.1:p.Cys65Arg
NM_001243036.1:c.193T>C	NP_001229965.1:p.Cys65Arg
NM_001243036.2:c.193T>C	NP_001229965.1:p.Cys65Arg
NM_014270.4:c.193T>C	NP_055085.1:p.Cys65Arg
ENST00000023064.8:c.193T>C	ENSP00000023064.3:p.Cys65Arg
ENST00000587772.1:c.193T>C	ENSP00000468439.1:p.Cys65Arg
ENST00000590341.5:c.193T>C	ENSP00000464822.1:p.Cys65Arg
ENST00000590465.5:c.88-333T>C	ENSP00000468076.1:n.88-333T>C
ENST00000592232.5:c.88-333T>C	ENSP00000465563.1:n.88-333T>C
XM_006722992.1:c.-263T>C	XP_006723055.1:n.-263T>C
XM_011526402.1:c.193T>C	XP_011524704.1:p.Cys65Arg
XM_011526402.3:c.193T>C	XP_011524704.1:p.Cys65Arg
XM_017026230.1:c.-29-333T>C	XP_016881719.1:n.-29-333T>C
XM_024451334.1:c.-850T>C	XP_024307102.1:n.-850T>C