Canonical Allele Identifier: CA1918678627

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362697_71362723delinsAAAGTTTCACTTGGGGACAGAGAGCAG , CM000672.2:g.71362697_71362723delinsAAAGTTTCACTTGGGGACAGAGAGCAG	GRCh38
NC_000010.10:g.73122454_73122480delinsAAAGTTTCACTTGGGGACAGAGAGCAG , CM000672.1:g.73122454_73122480delinsAAAGTTTCACTTGGGGACAGAGAGCAG	GRCh37
NC_000010.9:g.72792460_72792486delinsAAAGTTTCACTTGGGGACAGAGAGCAG	NCBI36
NG_017066.1:g.48445_48471delinsAAAGTTTCACTTGGGGACAGAGAGCAG
NG_017066.2:g.48439_48465delinsAAAGTTTCACTTGGGGACAGAGAGCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2993_3019delinsAAAGTTTCACTTGGGGACAGAGAGCAG
ENST00000373189.6:c.*89_*115delinsAAAGTTTCACTTGGGGACAGAGAGCAG MANE Select	ENSP00000362285.5:n.*89_*115delinsAAAGTTTCACTTGGGGACAGAGAGCAG...
ENST00000479577.2:c.*89_*115delinsAAAGTTTCACTTGGGGACAGAGAGCAG	ENSP00000493995.1:n.*89_*115delinsAAAGTTTCACTTGGGGACAGAGAGCAG...
ENST00000642198.1:c.*1089_*1115delinsAAAGTTTCACTTGGGGACAGAGAGCAG	ENSP00000494827.1:n.*1089_*1115delinsAAAGTTTCACTTGGGGACAGAGAG...
ENST00000642772.1:c.*94+6454_*94+6480delinsAAAGTTTCACTTGGGGACAGAGAGCAG	ENSP00000495041.1:n.*94+6454_*94+6480delinsAAAGTTTCACTTGGGGAC...
ENST00000643042.1:c.1138_1164delinsAAAGTTTCACTTGGGGACAGAGAGCAG	ENSP00000496674.1:n.1138_1164delinsAAAGTTTCACTTGGGGACAGAGAGCA...
ENST00000643619.1:c.*1100_*1126delinsAAAGTTTCACTTGGGGACAGAGAGCAG	ENSP00000494378.1:n.*1100_*1126delinsAAAGTTTCACTTGGGGACAGAGAG...
ENST00000643752.1:c.*843_*869delinsAAAGTTTCACTTGGGGACAGAGAGCAG	ENSP00000495000.1:n.*843_*869delinsAAAGTTTCACTTGGGGACAGAGAGCA...
ENST00000644088.1:c.*838_*864delinsAAAGTTTCACTTGGGGACAGAGAGCAG	ENSP00000494066.1:n.*838_*864delinsAAAGTTTCACTTGGGGACAGAGAGCA...
ENST00000644591.1:c.*843_*869delinsAAAGTTTCACTTGGGGACAGAGAGCAG	ENSP00000496664.1:n.*843_*869delinsAAAGTTTCACTTGGGGACAGAGAGCA...
ENST00000644895.1:c.*99+6454_*99+6480delinsAAAGTTTCACTTGGGGACAGAGAGCAG	ENSP00000493872.1:n.*99+6454_*99+6480delinsAAAGTTTCACTTGGGGAC...
ENST00000645345.1:c.*1089_*1115delinsAAAGTTTCACTTGGGGACAGAGAGCAG	ENSP00000495859.1:n.*1089_*1115delinsAAAGTTTCACTTGGGGACAGAGAG...
ENST00000647524.1:c.*1100_*1126delinsAAAGTTTCACTTGGGGACAGAGAGCAG	ENSP00000495077.1:n.*1100_*1126delinsAAAGTTTCACTTGGGGACAGAGAG...
ENST00000373189.5:c.*89_*115delinsAAAGTTTCACTTGGGGACAGAGAGCAG	ENSP00000362285.5:n.*89_*115delinsAAAGTTTCACTTGGGGACAGAGAGCAG...
NM_001174098.1:c.*746_*772delinsAAAGTTTCACTTGGGGACAGAGAGCAG	NP_001167569.1:n.*746_*772delinsAAAGTTTCACTTGGGGACAGAGAGCAG
NM_018344.5:c.*89_*115delinsAAAGTTTCACTTGGGGACAGAGAGCAG	NP_060814.4:n.*89_*115delinsAAAGTTTCACTTGGGGACAGAGAGCAG
NR_033413.1:n.1491_1517delinsAAAGTTTCACTTGGGGACAGAGAGCAG
NR_033414.1:n.1264_1290delinsAAAGTTTCACTTGGGGACAGAGAGCAG
XM_006717910.2:c.*89_*115delinsAAAGTTTCACTTGGGGACAGAGAGCAG	XP_006717973.1:n.*89_*115delinsAAAGTTTCACTTGGGGACAGAGAGCAG
NM_001363518.1:c.*89_*115delinsAAAGTTTCACTTGGGGACAGAGAGCAG	NP_001350447.1:n.*89_*115delinsAAAGTTTCACTTGGGGACAGAGAGCAG
XM_017016377.2:c.*89_*115delinsAAAGTTTCACTTGGGGACAGAGAGCAG	XP_016871866.1:n.*89_*115delinsAAAGTTTCACTTGGGGACAGAGAGCAG
XM_017016378.2:c.*89_*115delinsAAAGTTTCACTTGGGGACAGAGAGCAG	XP_016871867.1:n.*89_*115delinsAAAGTTTCACTTGGGGACAGAGAGCAG
NM_018344.6:c.*89_*115delinsAAAGTTTCACTTGGGGACAGAGAGCAG MANE Select	NP_060814.4:n.*89_*115delinsAAAGTTTCACTTGGGGACAGAGAGCAG
NM_001174098.2:c.*746_*772delinsAAAGTTTCACTTGGGGACAGAGAGCAG	NP_001167569.1:n.*746_*772delinsAAAGTTTCACTTGGGGACAGAGAGCAG
NM_001363518.2:c.*89_*115delinsAAAGTTTCACTTGGGGACAGAGAGCAG	NP_001350447.1:n.*89_*115delinsAAAGTTTCACTTGGGGACAGAGAGCAG
NR_033413.2:n.1485_1511delinsAAAGTTTCACTTGGGGACAGAGAGCAG
NR_033414.2:n.1258_1284delinsAAAGTTTCACTTGGGGACAGAGAGCAG