Canonical Allele Identifier: CA9358845

Gene: SLC7A9

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.32864155A>G , CM000681.2:g.32864155A>G	GRCh38
NC_000019.9:g.33355061A>G , CM000681.1:g.33355061A>G	GRCh37
NC_000019.8:g.38046901A>G	NCBI36
NG_008258.1:g.10623T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_014270.5:c.419T>C MANE Select	NP_055085.1:p.Phe140Ser
ENST00000023064.9:c.419T>C MANE Select	ENSP00000023064.3:p.Phe140Ser
NM_001126335.1:c.419T>C	NP_001119807.1:p.Phe140Ser
NM_001126335.2:c.419T>C	NP_001119807.1:p.Phe140Ser
NM_001243036.1:c.419T>C	NP_001229965.1:p.Phe140Ser
NM_001243036.2:c.419T>C	NP_001229965.1:p.Phe140Ser
NM_014270.4:c.419T>C	NP_055085.1:p.Phe140Ser
ENST00000023064.8:c.419T>C	ENSP00000023064.3:p.Phe140Ser
ENST00000587772.1:c.419T>C	ENSP00000468439.1:p.Phe140Ser
ENST00000589659.1:n.364T>C
ENST00000590341.5:c.419T>C	ENSP00000464822.1:p.Phe140Ser
ENST00000590465.5:c.*151T>C	ENSP00000468076.1:n.*151T>C
ENST00000592232.5:c.*151T>C	ENSP00000465563.1:n.*151T>C
XM_006722992.1:c.-37T>C	XP_006723055.1:n.-37T>C
XM_011526402.1:c.419T>C	XP_011524704.1:p.Phe140Ser
XM_011526402.3:c.419T>C	XP_011524704.1:p.Phe140Ser
XM_017026230.1:c.155T>C	XP_016881719.1:p.Phe52Ser
XM_024451334.1:c.-624T>C	XP_024307102.1:n.-624T>C