Canonical Allele Identifier: CA1918678295

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71361995G= , CM000672.2:g.71361995G=	GRCh38
NC_000010.10:g.73121752G= , CM000672.1:g.73121752G=	GRCh37
NC_000010.9:g.72791758G=	NCBI36
NG_017066.1:g.47743G=
NG_017066.2:g.47737G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2291G=
ENST00000373189.6:c.815G= MANE Select	ENSP00000362285.5:p.Gly272=
ENST00000479577.2:c.581G=	ENSP00000493995.1:p.Gly194=
ENST00000642198.1:c.*387G=	ENSP00000494827.1:n.*387G=
ENST00000642772.1:c.*94+5752G=	ENSP00000495041.1:n.*94+5752G=
ENST00000643042.1:c.436G=	ENSP00000496674.1:n.436G=
ENST00000643619.1:c.*398G=	ENSP00000494378.1:n.*398G=
ENST00000643752.1:c.*141G=	ENSP00000495000.1:n.*141G=
ENST00000644088.1:c.*136G=	ENSP00000494066.1:n.*136G=
ENST00000644591.1:c.*141G=	ENSP00000496664.1:n.*141G=
ENST00000644895.1:c.*99+5752G=	ENSP00000493872.1:n.*99+5752G=
ENST00000645345.1:c.*387G=	ENSP00000495859.1:n.*387G=
ENST00000647524.1:c.*398G=	ENSP00000495077.1:n.*398G=
ENST00000373189.5:c.815G=	ENSP00000362285.5:p.Gly272=
ENST00000469204.1:n.312G=
NM_001174098.1:c.*44G=	NP_001167569.1:n.*44G=
NM_018344.5:c.815G=	NP_060814.4:p.Gly272=
NR_033413.1:n.789G=
NR_033414.1:n.562G=
XM_006717910.2:c.581G=	XP_006717973.1:p.Gly194=
NM_001363518.1:c.581G=	NP_001350447.1:p.Gly194=
XM_017016377.2:c.377G=	XP_016871866.1:p.Gly126=
XM_017016378.2:c.197G=	XP_016871867.1:p.Gly66=
NM_018344.6:c.815G= MANE Select	NP_060814.4:p.Gly272=
NM_001174098.2:c.*44G=	NP_001167569.1:n.*44G=
NM_001363518.2:c.581G=	NP_001350447.1:p.Gly194=
NR_033413.2:n.783G=
NR_033414.2:n.556G=