Canonical Allele Identifier: CA1918678450

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362321G= , CM000672.2:g.71362321G=	GRCh38
NC_000010.10:g.73122078G= , CM000672.1:g.73122078G=	GRCh37
NC_000010.9:g.72792084G=	NCBI36
NG_017066.1:g.48069G=
NG_017066.2:g.48063G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2617G=
ENST00000373189.6:c.1141G= MANE Select	ENSP00000362285.5:p.Gly381=
ENST00000479577.2:c.907G=	ENSP00000493995.1:p.Gly303=
ENST00000642198.1:c.*713G=	ENSP00000494827.1:n.*713G=
ENST00000642772.1:c.*94+6078G=	ENSP00000495041.1:n.*94+6078G=
ENST00000643042.1:c.762G=	ENSP00000496674.1:n.762G=
ENST00000643619.1:c.*724G=	ENSP00000494378.1:n.*724G=
ENST00000643752.1:c.*467G=	ENSP00000495000.1:n.*467G=
ENST00000644088.1:c.*462G=	ENSP00000494066.1:n.*462G=
ENST00000644591.1:c.*467G=	ENSP00000496664.1:n.*467G=
ENST00000644895.1:c.*99+6078G=	ENSP00000493872.1:n.*99+6078G=
ENST00000645345.1:c.*713G=	ENSP00000495859.1:n.*713G=
ENST00000647524.1:c.*724G=	ENSP00000495077.1:n.*724G=
ENST00000373189.5:c.1141G=	ENSP00000362285.5:p.Gly381=
ENST00000469204.1:n.638G=
NM_001174098.1:c.*370G=	NP_001167569.1:n.*370G=
NM_018344.5:c.1141G=	NP_060814.4:p.Gly381=
NR_033413.1:n.1115G=
NR_033414.1:n.888G=
XM_006717910.2:c.907G=	XP_006717973.1:p.Gly303=
NM_001363518.1:c.907G=	NP_001350447.1:p.Gly303=
XM_017016377.2:c.703G=	XP_016871866.1:p.Gly235=
XM_017016378.2:c.523G=	XP_016871867.1:p.Gly175=
NM_018344.6:c.1141G= MANE Select	NP_060814.4:p.Gly381=
NM_001174098.2:c.*370G=	NP_001167569.1:n.*370G=
NM_001363518.2:c.907G=	NP_001350447.1:p.Gly303=
NR_033413.2:n.1109G=
NR_033414.2:n.882G=