Canonical Allele Identifier: CA470280759

Gene: SLC29A3

Linked Data

• dbSNP Id: rs1239572344
• MyVariant Identifiers: chr10:g.73121738C>T (hg19) ; chr10:g.71361981C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71361981C>T , CM000672.2:g.71361981C>T	GRCh38
NC_000010.10:g.73121738C>T , CM000672.1:g.73121738C>T	GRCh37
NC_000010.9:g.72791744C>T	NCBI36
NG_017066.1:g.47729C>T
NG_017066.2:g.47723C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2277C>T
ENST00000373189.6:c.801C>T MANE Select	ENSP00000362285.5:p.Ala267=
ENST00000479577.2:c.567C>T	ENSP00000493995.1:p.Ala189=
ENST00000642198.1:c.*373C>T	ENSP00000494827.1:n.*373C>T
ENST00000642772.1:c.*94+5738C>T	ENSP00000495041.1:n.*94+5738C>T
ENST00000643042.1:c.422C>T	ENSP00000496674.1:n.422C>T
ENST00000643619.1:c.*384C>T	ENSP00000494378.1:n.*384C>T
ENST00000643752.1:c.*127C>T	ENSP00000495000.1:n.*127C>T
ENST00000644088.1:c.*122C>T	ENSP00000494066.1:n.*122C>T
ENST00000644591.1:c.*127C>T	ENSP00000496664.1:n.*127C>T
ENST00000644895.1:c.*99+5738C>T	ENSP00000493872.1:n.*99+5738C>T
ENST00000645345.1:c.*373C>T	ENSP00000495859.1:n.*373C>T
ENST00000647524.1:c.*384C>T	ENSP00000495077.1:n.*384C>T
ENST00000373189.5:c.801C>T	ENSP00000362285.5:p.Ala267=
ENST00000469204.1:n.298C>T
NM_001174098.1:c.*30C>T	NP_001167569.1:n.*30C>T
NM_018344.5:c.801C>T	NP_060814.4:p.Ala267=
NR_033413.1:n.775C>T
NR_033414.1:n.548C>T
XM_006717910.2:c.567C>T	XP_006717973.1:p.Ala189=
NM_001363518.1:c.567C>T	NP_001350447.1:p.Ala189=
XM_017016377.2:c.363C>T	XP_016871866.1:p.Ala121=
XM_017016378.2:c.183C>T	XP_016871867.1:p.Ala61=
NM_018344.6:c.801C>T MANE Select	NP_060814.4:p.Ala267=
NM_001174098.2:c.*30C>T	NP_001167569.1:n.*30C>T
NM_001363518.2:c.567C>T	NP_001350447.1:p.Ala189=
NR_033413.2:n.769C>T
NR_033414.2:n.542C>T