Canonical Allele Identifier: CA405202462

Gene: SLC7A9

Linked Data

• MyVariant Identifiers: chr19:g.33353067T>A (hg19) ; chr19:g.32862161T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.32862161T>A , CM000681.2:g.32862161T>A	GRCh38
NC_000019.9:g.33353067T>A , CM000681.1:g.33353067T>A	GRCh37
NC_000019.8:g.38044907T>A	NCBI36
NG_008258.1:g.12617A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000023064.9:c.661A>T MANE Select	ENSP00000023064.3:p.Ile221Phe
ENST00000023064.8:c.661A>T	ENSP00000023064.3:p.Ile221Phe
ENST00000587772.1:c.661A>T	ENSP00000468439.1:p.Ile221Phe
ENST00000589659.1:n.606A>T
ENST00000590341.5:c.661A>T	ENSP00000464822.1:p.Ile221Phe
ENST00000590465.5:c.*211-1511A>T	ENSP00000468076.1:n.*211-1511A>T
ENST00000592232.5:c.*211-1511A>T	ENSP00000465563.1:n.*211-1511A>T
NM_001126335.1:c.661A>T	NP_001119807.1:p.Ile221Phe
NM_001243036.1:c.661A>T	NP_001229965.1:p.Ile221Phe
NM_014270.4:c.661A>T	NP_055085.1:p.Ile221Phe
XM_006722992.1:c.24-1511A>T	XP_006723055.1:n.24-1511A>T
XM_011526402.1:c.661A>T	XP_011524704.1:p.Ile221Phe
XM_011526402.3:c.661A>T	XP_011524704.1:p.Ile221Phe
XM_017026230.1:c.397A>T	XP_016881719.1:p.Ile133Phe
XM_024451334.1:c.-564-1511A>T	XP_024307102.1:n.-564-1511A>T
NM_014270.5:c.661A>T MANE Select	NP_055085.1:p.Ile221Phe
NM_001126335.2:c.661A>T	NP_001119807.1:p.Ile221Phe
NM_001243036.2:c.661A>T	NP_001229965.1:p.Ile221Phe