Canonical Allele Identifier: CA2609558662

Gene: SLC29A3

Linked Data

• gnomAD v4: 10-71362184-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362187dup , CM000672.2:g.71362187dup	GRCh38
NC_000010.10:g.73121944dup , CM000672.1:g.73121944dup	GRCh37
NC_000010.9:g.72791950dup	NCBI36
NG_017066.1:g.47935dup
NG_017066.2:g.47929dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2483dup
ENST00000373189.6:c.1007dup MANE Select	ENSP00000362285.5:p.Ser337PhefsTer23
ENST00000479577.2:c.773dup	ENSP00000493995.1:p.Ser259PhefsTer23
ENST00000642198.1:c.*579dup	ENSP00000494827.1:n.*579dup
ENST00000642772.1:c.*94+5944dup	ENSP00000495041.1:n.*94+5944dup
ENST00000643042.1:c.628dup	ENSP00000496674.1:n.628dup
ENST00000643619.1:c.*590dup	ENSP00000494378.1:n.*590dup
ENST00000643752.1:c.*333dup	ENSP00000495000.1:n.*333dup
ENST00000644088.1:c.*328dup	ENSP00000494066.1:n.*328dup
ENST00000644591.1:c.*333dup	ENSP00000496664.1:n.*333dup
ENST00000644895.1:c.*99+5944dup	ENSP00000493872.1:n.*99+5944dup
ENST00000645345.1:c.*579dup	ENSP00000495859.1:n.*579dup
ENST00000647524.1:c.*590dup	ENSP00000495077.1:n.*590dup
ENST00000373189.5:c.1007dup	ENSP00000362285.5:p.Ser337PhefsTer23
ENST00000469204.1:n.504dup
NM_001174098.1:c.*236dup	NP_001167569.1:n.*236dup
NM_018344.5:c.1007dup	NP_060814.4:p.Ser337PhefsTer23
NR_033413.1:n.981dup
NR_033414.1:n.754dup
XM_006717910.2:c.773dup	XP_006717973.1:p.Ser259PhefsTer23
NM_001363518.1:c.773dup	NP_001350447.1:p.Ser259PhefsTer23
XM_017016377.2:c.569dup	XP_016871866.1:p.Ser191PhefsTer23
XM_017016378.2:c.389dup	XP_016871867.1:p.Ser131PhefsTer23
NM_018344.6:c.1007dup MANE Select	NP_060814.4:p.Ser337PhefsTer23
NM_001174098.2:c.*236dup	NP_001167569.1:n.*236dup
NM_001363518.2:c.773dup	NP_001350447.1:p.Ser259PhefsTer23
NR_033413.2:n.975dup
NR_033414.2:n.748dup