Canonical Allele Identifier: CA2332455388
Gene: SLC7A9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.32862080A= , CM000681.2:g.32862080A= GRCh38
NC_000019.9:g.33352986A= , CM000681.1:g.33352986A= GRCh37
NC_000019.8:g.38044826A= NCBI36
NG_008258.1:g.12698T=

Transcript Alleles

HGVS Amino-acid change
ENST00000023064.9:c.704+38T= MANE Select ENSP00000023064.3:n.704+38T=
ENST00000023064.8:c.704+38T= ENSP00000023064.3:n.704+38T=
ENST00000587772.1:c.704+38T= ENSP00000468439.1:n.704+38T=
ENST00000589659.1:n.649+38T=
ENST00000590341.5:c.704+38T= ENSP00000464822.1:n.704+38T=
ENST00000590465.5:c.*211-1430T= ENSP00000468076.1:n.*211-1430T=
ENST00000592232.5:c.*211-1430T= ENSP00000465563.1:n.*211-1430T=
NM_001126335.1:c.704+38T= NP_001119807.1:n.704+38T=
NM_001243036.1:c.704+38T= NP_001229965.1:n.704+38T=
NM_014270.4:c.704+38T= NP_055085.1:n.704+38T=
XM_006722992.1:c.24-1430T= XP_006723055.1:n.24-1430T=
XM_011526402.1:c.704+38T= XP_011524704.1:n.704+38T=
XM_011526402.3:c.704+38T= XP_011524704.1:n.704+38T=
XM_017026230.1:c.440+38T= XP_016881719.1:n.440+38T=
XM_024451334.1:c.-564-1430T= XP_024307102.1:n.-564-1430T=
NM_014270.5:c.704+38T= MANE Select NP_055085.1:n.704+38T=
NM_001126335.2:c.704+38T= NP_001119807.1:n.704+38T=
NM_001243036.2:c.704+38T= NP_001229965.1:n.704+38T=