Canonical Allele Identifier: CA506666798

Gene: SLC7A9

Linked Data

• MyVariant Identifiers: chr19:g.33353074C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.32862168C>G , CM000681.2:g.32862168C>G	GRCh38
NC_000019.9:g.33353074C>G , CM000681.1:g.33353074C>G	GRCh37
NC_000019.8:g.38044914C>G	NCBI36
NG_008258.1:g.12610G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000023064.9:c.654G>C MANE Select	ENSP00000023064.3:p.Val218=
ENST00000023064.8:c.654G>C	ENSP00000023064.3:p.Val218=
ENST00000587772.1:c.654G>C	ENSP00000468439.1:p.Val218=
ENST00000589659.1:n.599G>C
ENST00000590341.5:c.654G>C	ENSP00000464822.1:p.Val218=
ENST00000590465.5:c.*211-1518G>C	ENSP00000468076.1:n.*211-1518G>C
ENST00000592232.5:c.*211-1518G>C	ENSP00000465563.1:n.*211-1518G>C
NM_001126335.1:c.654G>C	NP_001119807.1:p.Val218=
NM_001243036.1:c.654G>C	NP_001229965.1:p.Val218=
NM_014270.4:c.654G>C	NP_055085.1:p.Val218=
XM_006722992.1:c.24-1518G>C	XP_006723055.1:n.24-1518G>C
XM_011526402.1:c.654G>C	XP_011524704.1:p.Val218=
XM_011526402.3:c.654G>C	XP_011524704.1:p.Val218=
XM_017026230.1:c.390G>C	XP_016881719.1:p.Val130=
XM_024451334.1:c.-564-1518G>C	XP_024307102.1:n.-564-1518G>C
NM_014270.5:c.654G>C MANE Select	NP_055085.1:p.Val218=
NM_001126335.2:c.654G>C	NP_001119807.1:p.Val218=
NM_001243036.2:c.654G>C	NP_001229965.1:p.Val218=