Canonical Allele Identifier: CA377115679

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73121961A>T (hg19) ; chr10:g.71362204A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362204A>T , CM000672.2:g.71362204A>T	GRCh38
NC_000010.10:g.73121961A>T , CM000672.1:g.73121961A>T	GRCh37
NC_000010.9:g.72791967A>T	NCBI36
NG_017066.1:g.47952A>T
NG_017066.2:g.47946A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2500A>T
ENST00000373189.6:c.1024A>T MANE Select	ENSP00000362285.5:p.Thr342Ser
ENST00000479577.2:c.790A>T	ENSP00000493995.1:p.Thr264Ser
ENST00000642198.1:c.*596A>T	ENSP00000494827.1:n.*596A>T
ENST00000642772.1:c.*94+5961A>T	ENSP00000495041.1:n.*94+5961A>T
ENST00000643042.1:c.645A>T	ENSP00000496674.1:n.645A>T
ENST00000643619.1:c.*607A>T	ENSP00000494378.1:n.*607A>T
ENST00000643752.1:c.*350A>T	ENSP00000495000.1:n.*350A>T
ENST00000644088.1:c.*345A>T	ENSP00000494066.1:n.*345A>T
ENST00000644591.1:c.*350A>T	ENSP00000496664.1:n.*350A>T
ENST00000644895.1:c.*99+5961A>T	ENSP00000493872.1:n.*99+5961A>T
ENST00000645345.1:c.*596A>T	ENSP00000495859.1:n.*596A>T
ENST00000647524.1:c.*607A>T	ENSP00000495077.1:n.*607A>T
ENST00000373189.5:c.1024A>T	ENSP00000362285.5:p.Thr342Ser
ENST00000469204.1:n.521A>T
NM_001174098.1:c.*253A>T	NP_001167569.1:n.*253A>T
NM_018344.5:c.1024A>T	NP_060814.4:p.Thr342Ser
NR_033413.1:n.998A>T
NR_033414.1:n.771A>T
XM_006717910.2:c.790A>T	XP_006717973.1:p.Thr264Ser
NM_001363518.1:c.790A>T	NP_001350447.1:p.Thr264Ser
XM_017016377.2:c.586A>T	XP_016871866.1:p.Thr196Ser
XM_017016378.2:c.406A>T	XP_016871867.1:p.Thr136Ser
NM_018344.6:c.1024A>T MANE Select	NP_060814.4:p.Thr342Ser
NM_001174098.2:c.*253A>T	NP_001167569.1:n.*253A>T
NM_001363518.2:c.790A>T	NP_001350447.1:p.Thr264Ser
NR_033413.2:n.992A>T
NR_033414.2:n.765A>T