Canonical Allele Identifier: CA506666778

Gene: SLC7A9

Linked Data

• MyVariant Identifiers: chr19:g.33353044T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.32862138T>C , CM000681.2:g.32862138T>C	GRCh38
NC_000019.9:g.33353044T>C , CM000681.1:g.33353044T>C	GRCh37
NC_000019.8:g.38044884T>C	NCBI36
NG_008258.1:g.12640A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000023064.9:c.684A>G MANE Select	ENSP00000023064.3:p.Gly228=
ENST00000023064.8:c.684A>G	ENSP00000023064.3:p.Gly228=
ENST00000587772.1:c.684A>G	ENSP00000468439.1:p.Gly228=
ENST00000589659.1:n.629A>G
ENST00000590341.5:c.684A>G	ENSP00000464822.1:p.Gly228=
ENST00000590465.5:c.*211-1488A>G	ENSP00000468076.1:n.*211-1488A>G
ENST00000592232.5:c.*211-1488A>G	ENSP00000465563.1:n.*211-1488A>G
NM_001126335.1:c.684A>G	NP_001119807.1:p.Gly228=
NM_001243036.1:c.684A>G	NP_001229965.1:p.Gly228=
NM_014270.4:c.684A>G	NP_055085.1:p.Gly228=
XM_006722992.1:c.24-1488A>G	XP_006723055.1:n.24-1488A>G
XM_011526402.1:c.684A>G	XP_011524704.1:p.Gly228=
XM_011526402.3:c.684A>G	XP_011524704.1:p.Gly228=
XM_017026230.1:c.420A>G	XP_016881719.1:p.Gly140=
XM_024451334.1:c.-564-1488A>G	XP_024307102.1:n.-564-1488A>G
NM_014270.5:c.684A>G MANE Select	NP_055085.1:p.Gly228=
NM_001126335.2:c.684A>G	NP_001119807.1:p.Gly228=
NM_001243036.2:c.684A>G	NP_001229965.1:p.Gly228=