Canonical Allele Identifier: CA1918678600

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362639_71362648delinsGAGCCTTTGA , CM000672.2:g.71362639_71362648delinsGAGCCTTTGA	GRCh38
NC_000010.10:g.73122396_73122405delinsGAGCCTTTGA , CM000672.1:g.73122396_73122405delinsGAGCCTTTGA	GRCh37
NC_000010.9:g.72792402_72792411delinsGAGCCTTTGA	NCBI36
NG_017066.1:g.48387_48396delinsGAGCCTTTGA
NG_017066.2:g.48381_48390delinsGAGCCTTTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2935_2944delinsGAGCCTTTGA
ENST00000373189.6:c.*31_*40delinsGAGCCTTTGA MANE Select	ENSP00000362285.5:n.*31_*40delinsGAGCCTTTGA
ENST00000479577.2:c.*31_*40delinsGAGCCTTTGA	ENSP00000493995.1:n.*31_*40delinsGAGCCTTTGA
ENST00000642198.1:c.*1031_*1040delinsGAGCCTTTGA	ENSP00000494827.1:n.*1031_*1040delinsGAGCCTTTGA
ENST00000642772.1:c.*94+6396_*94+6405delinsGAGCCTTTGA	ENSP00000495041.1:n.*94+6396_*94+6405delinsGAGCCTTTGA
ENST00000643042.1:c.1080_1089delinsGAGCCTTTGA	ENSP00000496674.1:n.1080_1089delinsGAGCCTTTGA
ENST00000643619.1:c.*1042_*1051delinsGAGCCTTTGA	ENSP00000494378.1:n.*1042_*1051delinsGAGCCTTTGA
ENST00000643752.1:c.*785_*794delinsGAGCCTTTGA	ENSP00000495000.1:n.*785_*794delinsGAGCCTTTGA
ENST00000644088.1:c.*780_*789delinsGAGCCTTTGA	ENSP00000494066.1:n.*780_*789delinsGAGCCTTTGA
ENST00000644591.1:c.*785_*794delinsGAGCCTTTGA	ENSP00000496664.1:n.*785_*794delinsGAGCCTTTGA
ENST00000644895.1:c.*99+6396_*99+6405delinsGAGCCTTTGA	ENSP00000493872.1:n.*99+6396_*99+6405delinsGAGCCTTTGA
ENST00000645345.1:c.*1031_*1040delinsGAGCCTTTGA	ENSP00000495859.1:n.*1031_*1040delinsGAGCCTTTGA
ENST00000647524.1:c.*1042_*1051delinsGAGCCTTTGA	ENSP00000495077.1:n.*1042_*1051delinsGAGCCTTTGA
ENST00000373189.5:c.*31_*40delinsGAGCCTTTGA	ENSP00000362285.5:n.*31_*40delinsGAGCCTTTGA
NM_001174098.1:c.*688_*697delinsGAGCCTTTGA	NP_001167569.1:n.*688_*697delinsGAGCCTTTGA
NM_018344.5:c.*31_*40delinsGAGCCTTTGA	NP_060814.4:n.*31_*40delinsGAGCCTTTGA
NR_033413.1:n.1433_1442delinsGAGCCTTTGA
NR_033414.1:n.1206_1215delinsGAGCCTTTGA
XM_006717910.2:c.*31_*40delinsGAGCCTTTGA	XP_006717973.1:n.*31_*40delinsGAGCCTTTGA
NM_001363518.1:c.*31_*40delinsGAGCCTTTGA	NP_001350447.1:n.*31_*40delinsGAGCCTTTGA
XM_017016377.2:c.*31_*40delinsGAGCCTTTGA	XP_016871866.1:n.*31_*40delinsGAGCCTTTGA
XM_017016378.2:c.*31_*40delinsGAGCCTTTGA	XP_016871867.1:n.*31_*40delinsGAGCCTTTGA
NM_018344.6:c.*31_*40delinsGAGCCTTTGA MANE Select	NP_060814.4:n.*31_*40delinsGAGCCTTTGA
NM_001174098.2:c.*688_*697delinsGAGCCTTTGA	NP_001167569.1:n.*688_*697delinsGAGCCTTTGA
NM_001363518.2:c.*31_*40delinsGAGCCTTTGA	NP_001350447.1:n.*31_*40delinsGAGCCTTTGA
NR_033413.2:n.1427_1436delinsGAGCCTTTGA
NR_033414.2:n.1200_1209delinsGAGCCTTTGA