Canonical Allele Identifier: CA1918678362

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362135A= , CM000672.2:g.71362135A=	GRCh38
NC_000010.10:g.73121892A= , CM000672.1:g.73121892A=	GRCh37
NC_000010.9:g.72791898A=	NCBI36
NG_017066.1:g.47883A=
NG_017066.2:g.47877A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2431A=
ENST00000373189.6:c.955A= MANE Select	ENSP00000362285.5:p.Thr319=
ENST00000479577.2:c.721A=	ENSP00000493995.1:p.Thr241=
ENST00000642198.1:c.*527A=	ENSP00000494827.1:n.*527A=
ENST00000642772.1:c.*94+5892A=	ENSP00000495041.1:n.*94+5892A=
ENST00000643042.1:c.576A=	ENSP00000496674.1:n.576A=
ENST00000643619.1:c.*538A=	ENSP00000494378.1:n.*538A=
ENST00000643752.1:c.*281A=	ENSP00000495000.1:n.*281A=
ENST00000644088.1:c.*276A=	ENSP00000494066.1:n.*276A=
ENST00000644591.1:c.*281A=	ENSP00000496664.1:n.*281A=
ENST00000644895.1:c.*99+5892A=	ENSP00000493872.1:n.*99+5892A=
ENST00000645345.1:c.*527A=	ENSP00000495859.1:n.*527A=
ENST00000647524.1:c.*538A=	ENSP00000495077.1:n.*538A=
ENST00000373189.5:c.955A=	ENSP00000362285.5:p.Thr319=
ENST00000469204.1:n.452A=
NM_001174098.1:c.*184A=	NP_001167569.1:n.*184A=
NM_018344.5:c.955A=	NP_060814.4:p.Thr319=
NR_033413.1:n.929A=
NR_033414.1:n.702A=
XM_006717910.2:c.721A=	XP_006717973.1:p.Thr241=
NM_001363518.1:c.721A=	NP_001350447.1:p.Thr241=
XM_017016377.2:c.517A=	XP_016871866.1:p.Thr173=
XM_017016378.2:c.337A=	XP_016871867.1:p.Thr113=
NM_018344.6:c.955A= MANE Select	NP_060814.4:p.Thr319=
NM_001174098.2:c.*184A=	NP_001167569.1:n.*184A=
NM_001363518.2:c.721A=	NP_001350447.1:p.Thr241=
NR_033413.2:n.923A=
NR_033414.2:n.696A=