Canonical Allele Identifier: CA405202454
Gene: SLC7A9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.32862158T>A , CM000681.2:g.32862158T>A GRCh38
NC_000019.9:g.33353064T>A , CM000681.1:g.33353064T>A GRCh37
NC_000019.8:g.38044904T>A NCBI36
NG_008258.1:g.12620A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000023064.9:c.664A>T MANE Select ENSP00000023064.3:p.Ser222Cys
ENST00000023064.8:c.664A>T ENSP00000023064.3:p.Ser222Cys
ENST00000587772.1:c.664A>T ENSP00000468439.1:p.Ser222Cys
ENST00000589659.1:n.609A>T
ENST00000590341.5:c.664A>T ENSP00000464822.1:p.Ser222Cys
ENST00000590465.5:c.*211-1508A>T ENSP00000468076.1:n.*211-1508A>T
ENST00000592232.5:c.*211-1508A>T ENSP00000465563.1:n.*211-1508A>T
NM_001126335.1:c.664A>T NP_001119807.1:p.Ser222Cys
NM_001243036.1:c.664A>T NP_001229965.1:p.Ser222Cys
NM_014270.4:c.664A>T NP_055085.1:p.Ser222Cys
XM_006722992.1:c.24-1508A>T XP_006723055.1:n.24-1508A>T
XM_011526402.1:c.664A>T XP_011524704.1:p.Ser222Cys
XM_011526402.3:c.664A>T XP_011524704.1:p.Ser222Cys
XM_017026230.1:c.400A>T XP_016881719.1:p.Ser134Cys
XM_024451334.1:c.-564-1508A>T XP_024307102.1:n.-564-1508A>T
NM_014270.5:c.664A>T MANE Select NP_055085.1:p.Ser222Cys
NM_001126335.2:c.664A>T NP_001119807.1:p.Ser222Cys
NM_001243036.2:c.664A>T NP_001229965.1:p.Ser222Cys