Canonical Allele Identifier: CA2332455353

Gene: SLC7A9

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.32861974_32861975delinsCA , CM000681.2:g.32861974_32861975delinsCA	GRCh38
NC_000019.9:g.33352880_33352881delinsCA , CM000681.1:g.33352880_33352881delinsCA	GRCh37
NC_000019.8:g.38044720_38044721delinsCA	NCBI36
NG_008258.1:g.12803_12804delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000023064.9:c.704+143_704+144delinsTG MANE Select	ENSP00000023064.3:n.704+143_704+144delinsTG
ENST00000023064.8:c.704+143_704+144delinsTG	ENSP00000023064.3:n.704+143_704+144delinsTG
ENST00000587772.1:c.704+143_704+144delinsTG	ENSP00000468439.1:n.704+143_704+144delinsTG
ENST00000589659.1:n.649+143_649+144delinsTG
ENST00000590341.5:c.704+143_704+144delinsTG	ENSP00000464822.1:n.704+143_704+144delinsTG
ENST00000590465.5:c.*211-1325_*211-1324delinsTG	ENSP00000468076.1:n.*211-1325_*211-1324delinsTG
ENST00000592232.5:c.*211-1325_*211-1324delinsTG	ENSP00000465563.1:n.*211-1325_*211-1324delinsTG
NM_001126335.1:c.704+143_704+144delinsTG	NP_001119807.1:n.704+143_704+144delinsTG
NM_001243036.1:c.704+143_704+144delinsTG	NP_001229965.1:n.704+143_704+144delinsTG
NM_014270.4:c.704+143_704+144delinsTG	NP_055085.1:n.704+143_704+144delinsTG
XM_006722992.1:c.24-1325_24-1324delinsTG	XP_006723055.1:n.24-1325_24-1324delinsTG
XM_011526402.1:c.704+143_704+144delinsTG	XP_011524704.1:n.704+143_704+144delinsTG
XM_011526402.3:c.704+143_704+144delinsTG	XP_011524704.1:n.704+143_704+144delinsTG
XM_017026230.1:c.440+143_440+144delinsTG	XP_016881719.1:n.440+143_440+144delinsTG
XM_024451334.1:c.-564-1325_-564-1324delinsTG	XP_024307102.1:n.-564-1325_-564-1324delinsTG
NM_014270.5:c.704+143_704+144delinsTG MANE Select	NP_055085.1:n.704+143_704+144delinsTG
NM_001126335.2:c.704+143_704+144delinsTG	NP_001119807.1:n.704+143_704+144delinsTG
NM_001243036.2:c.704+143_704+144delinsTG	NP_001229965.1:n.704+143_704+144delinsTG