Canonical Allele Identifier: CA405202366

Gene: SLC7A9

Linked Data

• gnomAD v4: 19-32862122-C-T
• MyVariant Identifiers: chr19:g.33353028C>T (hg19) ; chr19:g.32862122C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.32862122C>T , CM000681.2:g.32862122C>T	GRCh38
NC_000019.9:g.33353028C>T , CM000681.1:g.33353028C>T	GRCh37
NC_000019.8:g.38044868C>T	NCBI36
NG_008258.1:g.12656G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000023064.9:c.700G>A MANE Select	ENSP00000023064.3:p.Gly234Arg
ENST00000023064.8:c.700G>A	ENSP00000023064.3:p.Gly234Arg
ENST00000587772.1:c.700G>A	ENSP00000468439.1:p.Gly234Arg
ENST00000589659.1:n.645G>A
ENST00000590341.5:c.700G>A	ENSP00000464822.1:p.Gly234Arg
ENST00000590465.5:c.*211-1472G>A	ENSP00000468076.1:n.*211-1472G>A
ENST00000592232.5:c.*211-1472G>A	ENSP00000465563.1:n.*211-1472G>A
NM_001126335.1:c.700G>A	NP_001119807.1:p.Gly234Arg
NM_001243036.1:c.700G>A	NP_001229965.1:p.Gly234Arg
NM_014270.4:c.700G>A	NP_055085.1:p.Gly234Arg
XM_006722992.1:c.24-1472G>A	XP_006723055.1:n.24-1472G>A
XM_011526402.1:c.700G>A	XP_011524704.1:p.Gly234Arg
XM_011526402.3:c.700G>A	XP_011524704.1:p.Gly234Arg
XM_017026230.1:c.436G>A	XP_016881719.1:p.Gly146Arg
XM_024451334.1:c.-564-1472G>A	XP_024307102.1:n.-564-1472G>A
NM_014270.5:c.700G>A MANE Select	NP_055085.1:p.Gly234Arg
NM_001126335.2:c.700G>A	NP_001119807.1:p.Gly234Arg
NM_001243036.2:c.700G>A	NP_001229965.1:p.Gly234Arg