Canonical Allele Identifier: CA470281130

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73121885C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362128C>T , CM000672.2:g.71362128C>T	GRCh38
NC_000010.10:g.73121885C>T , CM000672.1:g.73121885C>T	GRCh37
NC_000010.9:g.72791891C>T	NCBI36
NG_017066.1:g.47876C>T
NG_017066.2:g.47870C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2424C>T
ENST00000373189.6:c.948C>T MANE Select	ENSP00000362285.5:p.Phe316=
ENST00000479577.2:c.714C>T	ENSP00000493995.1:p.Phe238=
ENST00000642198.1:c.*520C>T	ENSP00000494827.1:n.*520C>T
ENST00000642772.1:c.*94+5885C>T	ENSP00000495041.1:n.*94+5885C>T
ENST00000643042.1:c.569C>T	ENSP00000496674.1:n.569C>T
ENST00000643619.1:c.*531C>T	ENSP00000494378.1:n.*531C>T
ENST00000643752.1:c.*274C>T	ENSP00000495000.1:n.*274C>T
ENST00000644088.1:c.*269C>T	ENSP00000494066.1:n.*269C>T
ENST00000644591.1:c.*274C>T	ENSP00000496664.1:n.*274C>T
ENST00000644895.1:c.*99+5885C>T	ENSP00000493872.1:n.*99+5885C>T
ENST00000645345.1:c.*520C>T	ENSP00000495859.1:n.*520C>T
ENST00000647524.1:c.*531C>T	ENSP00000495077.1:n.*531C>T
ENST00000373189.5:c.948C>T	ENSP00000362285.5:p.Phe316=
ENST00000469204.1:n.445C>T
NM_001174098.1:c.*177C>T	NP_001167569.1:n.*177C>T
NM_018344.5:c.948C>T	NP_060814.4:p.Phe316=
NR_033413.1:n.922C>T
NR_033414.1:n.695C>T
XM_006717910.2:c.714C>T	XP_006717973.1:p.Phe238=
NM_001363518.1:c.714C>T	NP_001350447.1:p.Phe238=
XM_017016377.2:c.510C>T	XP_016871866.1:p.Phe170=
XM_017016378.2:c.330C>T	XP_016871867.1:p.Phe110=
NM_018344.6:c.948C>T MANE Select	NP_060814.4:p.Phe316=
NM_001174098.2:c.*177C>T	NP_001167569.1:n.*177C>T
NM_001363518.2:c.714C>T	NP_001350447.1:p.Phe238=
NR_033413.2:n.916C>T
NR_033414.2:n.689C>T