Canonical Allele Identifier: CA1918678360

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362126T= , CM000672.2:g.71362126T=	GRCh38
NC_000010.10:g.73121883T= , CM000672.1:g.73121883T=	GRCh37
NC_000010.9:g.72791889T=	NCBI36
NG_017066.1:g.47874T=
NG_017066.2:g.47868T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2422T=
ENST00000373189.6:c.946T= MANE Select	ENSP00000362285.5:p.Phe316=
ENST00000479577.2:c.712T=	ENSP00000493995.1:p.Phe238=
ENST00000642198.1:c.*518T=	ENSP00000494827.1:n.*518T=
ENST00000642772.1:c.*94+5883T=	ENSP00000495041.1:n.*94+5883T=
ENST00000643042.1:c.567T=	ENSP00000496674.1:n.567T=
ENST00000643619.1:c.*529T=	ENSP00000494378.1:n.*529T=
ENST00000643752.1:c.*272T=	ENSP00000495000.1:n.*272T=
ENST00000644088.1:c.*267T=	ENSP00000494066.1:n.*267T=
ENST00000644591.1:c.*272T=	ENSP00000496664.1:n.*272T=
ENST00000644895.1:c.*99+5883T=	ENSP00000493872.1:n.*99+5883T=
ENST00000645345.1:c.*518T=	ENSP00000495859.1:n.*518T=
ENST00000647524.1:c.*529T=	ENSP00000495077.1:n.*529T=
ENST00000373189.5:c.946T=	ENSP00000362285.5:p.Phe316=
ENST00000469204.1:n.443T=
NM_001174098.1:c.*175T=	NP_001167569.1:n.*175T=
NM_018344.5:c.946T=	NP_060814.4:p.Phe316=
NR_033413.1:n.920T=
NR_033414.1:n.693T=
XM_006717910.2:c.712T=	XP_006717973.1:p.Phe238=
NM_001363518.1:c.712T=	NP_001350447.1:p.Phe238=
XM_017016377.2:c.508T=	XP_016871866.1:p.Phe170=
XM_017016378.2:c.328T=	XP_016871867.1:p.Phe110=
NM_018344.6:c.946T= MANE Select	NP_060814.4:p.Phe316=
NM_001174098.2:c.*175T=	NP_001167569.1:n.*175T=
NM_001363518.2:c.712T=	NP_001350447.1:p.Phe238=
NR_033413.2:n.914T=
NR_033414.2:n.687T=