Canonical Allele Identifier: CA405198118

Gene: SLC7A9

Linked Data

• MyVariant Identifiers: chr19:g.33333163T>G (hg19) ; chr19:g.32842257T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.32842257T>G , CM000681.2:g.32842257T>G	GRCh38
NC_000019.9:g.33333163T>G , CM000681.1:g.33333163T>G	GRCh37
NC_000019.8:g.38025003T>G	NCBI36
NG_008258.1:g.32521A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000023064.9:c.1135A>C MANE Select	ENSP00000023064.3:p.Ser379Arg
ENST00000023064.8:c.1135A>C	ENSP00000023064.3:p.Ser379Arg
ENST00000587772.1:c.1135A>C	ENSP00000468439.1:p.Ser379Arg
ENST00000590341.5:c.1135A>C	ENSP00000464822.1:p.Ser379Arg
ENST00000590465.5:c.*1282A>C	ENSP00000468076.1:n.*1282A>C
ENST00000592232.5:c.*544A>C	ENSP00000465563.1:n.*544A>C
NM_001126335.1:c.1135A>C	NP_001119807.1:p.Ser379Arg
NM_001243036.1:c.1135A>C	NP_001229965.1:p.Ser379Arg
NM_014270.4:c.1135A>C	NP_055085.1:p.Ser379Arg
XM_006722992.1:c.454A>C	XP_006723055.1:p.Ser152Arg
XM_011526402.1:c.1135A>C	XP_011524704.1:p.Ser379Arg
XM_011526402.3:c.1135A>C	XP_011524704.1:p.Ser379Arg
XM_017026230.1:c.871A>C	XP_016881719.1:p.Ser291Arg
XM_024451334.1:c.508A>C	XP_024307102.1:p.Ser170Arg
NM_014270.5:c.1135A>C MANE Select	NP_055085.1:p.Ser379Arg
NM_001126335.2:c.1135A>C	NP_001119807.1:p.Ser379Arg
NM_001243036.2:c.1135A>C	NP_001229965.1:p.Ser379Arg