Canonical Allele Identifier: CA405202475

Gene: SLC7A9

Linked Data

• MyVariant Identifiers: chr19:g.33353072C>A (hg19) ; chr19:g.32862166C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.32862166C>A , CM000681.2:g.32862166C>A	GRCh38
NC_000019.9:g.33353072C>A , CM000681.1:g.33353072C>A	GRCh37
NC_000019.8:g.38044912C>A	NCBI36
NG_008258.1:g.12612G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000023064.9:c.656G>T MANE Select	ENSP00000023064.3:p.Gly219Val
ENST00000023064.8:c.656G>T	ENSP00000023064.3:p.Gly219Val
ENST00000587772.1:c.656G>T	ENSP00000468439.1:p.Gly219Val
ENST00000589659.1:n.601G>T
ENST00000590341.5:c.656G>T	ENSP00000464822.1:p.Gly219Val
ENST00000590465.5:c.*211-1516G>T	ENSP00000468076.1:n.*211-1516G>T
ENST00000592232.5:c.*211-1516G>T	ENSP00000465563.1:n.*211-1516G>T
NM_001126335.1:c.656G>T	NP_001119807.1:p.Gly219Val
NM_001243036.1:c.656G>T	NP_001229965.1:p.Gly219Val
NM_014270.4:c.656G>T	NP_055085.1:p.Gly219Val
XM_006722992.1:c.24-1516G>T	XP_006723055.1:n.24-1516G>T
XM_011526402.1:c.656G>T	XP_011524704.1:p.Gly219Val
XM_011526402.3:c.656G>T	XP_011524704.1:p.Gly219Val
XM_017026230.1:c.392G>T	XP_016881719.1:p.Gly131Val
XM_024451334.1:c.-564-1516G>T	XP_024307102.1:n.-564-1516G>T
NM_014270.5:c.656G>T MANE Select	NP_055085.1:p.Gly219Val
NM_001126335.2:c.656G>T	NP_001119807.1:p.Gly219Val
NM_001243036.2:c.656G>T	NP_001229965.1:p.Gly219Val