Canonical Allele Identifier: CA377114305

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73121802A>T (hg19) ; chr10:g.71362045A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362045A>T , CM000672.2:g.71362045A>T	GRCh38
NC_000010.10:g.73121802A>T , CM000672.1:g.73121802A>T	GRCh37
NC_000010.9:g.72791808A>T	NCBI36
NG_017066.1:g.47793A>T
NG_017066.2:g.47787A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2341A>T
ENST00000373189.6:c.865A>T MANE Select	ENSP00000362285.5:p.Arg289Ter
ENST00000479577.2:c.631A>T	ENSP00000493995.1:p.Arg211Ter
ENST00000642198.1:c.*437A>T	ENSP00000494827.1:n.*437A>T
ENST00000642772.1:c.*94+5802A>T	ENSP00000495041.1:n.*94+5802A>T
ENST00000643042.1:c.486A>T	ENSP00000496674.1:n.486A>T
ENST00000643619.1:c.*448A>T	ENSP00000494378.1:n.*448A>T
ENST00000643752.1:c.*191A>T	ENSP00000495000.1:n.*191A>T
ENST00000644088.1:c.*186A>T	ENSP00000494066.1:n.*186A>T
ENST00000644591.1:c.*191A>T	ENSP00000496664.1:n.*191A>T
ENST00000644895.1:c.*99+5802A>T	ENSP00000493872.1:n.*99+5802A>T
ENST00000645345.1:c.*437A>T	ENSP00000495859.1:n.*437A>T
ENST00000647524.1:c.*448A>T	ENSP00000495077.1:n.*448A>T
ENST00000373189.5:c.865A>T	ENSP00000362285.5:p.Arg289Ter
ENST00000469204.1:n.362A>T
NM_001174098.1:c.*94A>T	NP_001167569.1:n.*94A>T
NM_018344.5:c.865A>T	NP_060814.4:p.Arg289Ter
NR_033413.1:n.839A>T
NR_033414.1:n.612A>T
XM_006717910.2:c.631A>T	XP_006717973.1:p.Arg211Ter
NM_001363518.1:c.631A>T	NP_001350447.1:p.Arg211Ter
XM_017016377.2:c.427A>T	XP_016871866.1:p.Arg143Ter
XM_017016378.2:c.247A>T	XP_016871867.1:p.Arg83Ter
NM_018344.6:c.865A>T MANE Select	NP_060814.4:p.Arg289Ter
NM_001174098.2:c.*94A>T	NP_001167569.1:n.*94A>T
NM_001363518.2:c.631A>T	NP_001350447.1:p.Arg211Ter
NR_033413.2:n.833A>T
NR_033414.2:n.606A>T