Canonical Allele Identifier: CA9358625

Gene: SLC7A9

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.32859901G>A , CM000681.2:g.32859901G>A	GRCh38
NC_000019.9:g.33350807G>A , CM000681.1:g.33350807G>A	GRCh37
NC_000019.8:g.38042647G>A	NCBI36
NG_008258.1:g.14877C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_014270.5:c.813C>T MANE Select	NP_055085.1:p.Asn271=
ENST00000023064.9:c.813C>T MANE Select	ENSP00000023064.3:p.Asn271=
NM_001126335.1:c.813C>T	NP_001119807.1:p.Asn271=
NM_001126335.2:c.813C>T	NP_001119807.1:p.Asn271=
NM_001243036.1:c.813C>T	NP_001229965.1:p.Asn271=
NM_001243036.2:c.813C>T	NP_001229965.1:p.Asn271=
NM_014270.4:c.813C>T	NP_055085.1:p.Asn271=
ENST00000023064.8:c.813C>T	ENSP00000023064.3:p.Asn271=
ENST00000587772.1:c.813C>T	ENSP00000468439.1:p.Asn271=
ENST00000589659.1:n.758C>T
ENST00000590341.5:c.813C>T	ENSP00000464822.1:p.Asn271=
ENST00000590465.5:c.*960C>T	ENSP00000468076.1:n.*960C>T
ENST00000592232.5:c.*319C>T	ENSP00000465563.1:n.*319C>T
XM_006722992.1:c.132C>T	XP_006723055.1:p.Asn44=
XM_011526402.1:c.813C>T	XP_011524704.1:p.Asn271=
XM_011526402.3:c.813C>T	XP_011524704.1:p.Asn271=
XM_017026230.1:c.549C>T	XP_016881719.1:p.Asn183=
XM_024451334.1:c.186C>T	XP_024307102.1:p.Asn62=