Canonical Allele Identifier: CA377113847

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73121736G>T (hg19) ; chr10:g.71361979G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71361979G>T , CM000672.2:g.71361979G>T	GRCh38
NC_000010.10:g.73121736G>T , CM000672.1:g.73121736G>T	GRCh37
NC_000010.9:g.72791742G>T	NCBI36
NG_017066.1:g.47727G>T
NG_017066.2:g.47721G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2275G>T
ENST00000373189.6:c.799G>T MANE Select	ENSP00000362285.5:p.Ala267Ser
ENST00000479577.2:c.565G>T	ENSP00000493995.1:p.Ala189Ser
ENST00000642198.1:c.*371G>T	ENSP00000494827.1:n.*371G>T
ENST00000642772.1:c.*94+5736G>T	ENSP00000495041.1:n.*94+5736G>T
ENST00000643042.1:c.420G>T	ENSP00000496674.1:n.420G>T
ENST00000643619.1:c.*382G>T	ENSP00000494378.1:n.*382G>T
ENST00000643752.1:c.*125G>T	ENSP00000495000.1:n.*125G>T
ENST00000644088.1:c.*120G>T	ENSP00000494066.1:n.*120G>T
ENST00000644591.1:c.*125G>T	ENSP00000496664.1:n.*125G>T
ENST00000644895.1:c.*99+5736G>T	ENSP00000493872.1:n.*99+5736G>T
ENST00000645345.1:c.*371G>T	ENSP00000495859.1:n.*371G>T
ENST00000647524.1:c.*382G>T	ENSP00000495077.1:n.*382G>T
ENST00000373189.5:c.799G>T	ENSP00000362285.5:p.Ala267Ser
ENST00000469204.1:n.296G>T
NM_001174098.1:c.*28G>T	NP_001167569.1:n.*28G>T
NM_018344.5:c.799G>T	NP_060814.4:p.Ala267Ser
NR_033413.1:n.773G>T
NR_033414.1:n.546G>T
XM_006717910.2:c.565G>T	XP_006717973.1:p.Ala189Ser
NM_001363518.1:c.565G>T	NP_001350447.1:p.Ala189Ser
XM_017016377.2:c.361G>T	XP_016871866.1:p.Ala121Ser
XM_017016378.2:c.181G>T	XP_016871867.1:p.Ala61Ser
NM_018344.6:c.799G>T MANE Select	NP_060814.4:p.Ala267Ser
NM_001174098.2:c.*28G>T	NP_001167569.1:n.*28G>T
NM_001363518.2:c.565G>T	NP_001350447.1:p.Ala189Ser
NR_033413.2:n.767G>T
NR_033414.2:n.540G>T