Canonical Allele Identifier: CA2609558753

Gene: SLC29A3

Linked Data

• gnomAD v4: 10-71362747-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362747C>T , CM000672.2:g.71362747C>T	GRCh38
NC_000010.10:g.73122504C>T , CM000672.1:g.73122504C>T	GRCh37
NC_000010.9:g.72792510C>T	NCBI36
NG_017066.1:g.48495C>T
NG_017066.2:g.48489C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.3043C>T
ENST00000373189.6:c.*139C>T MANE Select	ENSP00000362285.5:n.*139C>T
ENST00000479577.2:c.*139C>T	ENSP00000493995.1:n.*139C>T
ENST00000642198.1:c.*1139C>T	ENSP00000494827.1:n.*1139C>T
ENST00000642772.1:c.*94+6504C>T	ENSP00000495041.1:n.*94+6504C>T
ENST00000643042.1:c.1188C>T	ENSP00000496674.1:n.1188C>T
ENST00000643619.1:c.*1150C>T	ENSP00000494378.1:n.*1150C>T
ENST00000643752.1:c.*893C>T	ENSP00000495000.1:n.*893C>T
ENST00000644088.1:c.*888C>T	ENSP00000494066.1:n.*888C>T
ENST00000644591.1:c.*893C>T	ENSP00000496664.1:n.*893C>T
ENST00000644895.1:c.*99+6504C>T	ENSP00000493872.1:n.*99+6504C>T
ENST00000645345.1:c.*1139C>T	ENSP00000495859.1:n.*1139C>T
ENST00000647524.1:c.*1150C>T	ENSP00000495077.1:n.*1150C>T
ENST00000373189.5:c.*139C>T	ENSP00000362285.5:n.*139C>T
NM_001174098.1:c.*796C>T	NP_001167569.1:n.*796C>T
NM_018344.5:c.*139C>T	NP_060814.4:n.*139C>T
NR_033413.1:n.1541C>T
NR_033414.1:n.1314C>T
XM_006717910.2:c.*139C>T	XP_006717973.1:n.*139C>T
NM_001363518.1:c.*139C>T	NP_001350447.1:n.*139C>T
XM_017016377.2:c.*139C>T	XP_016871866.1:n.*139C>T
XM_017016378.2:c.*139C>T	XP_016871867.1:n.*139C>T
NM_018344.6:c.*139C>T MANE Select	NP_060814.4:n.*139C>T
NM_001174098.2:c.*796C>T	NP_001167569.1:n.*796C>T
NM_001363518.2:c.*139C>T	NP_001350447.1:n.*139C>T
NR_033413.2:n.1535C>T
NR_033414.2:n.1308C>T