Canonical Allele Identifier: CA1918678331

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362070C= , CM000672.2:g.71362070C=	GRCh38
NC_000010.10:g.73121827C= , CM000672.1:g.73121827C=	GRCh37
NC_000010.9:g.72791833C=	NCBI36
NG_017066.1:g.47818C=
NG_017066.2:g.47812C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2366C=
ENST00000373189.6:c.890C= MANE Select	ENSP00000362285.5:p.Pro297=
ENST00000479577.2:c.656C=	ENSP00000493995.1:p.Pro219=
ENST00000642198.1:c.*462C=	ENSP00000494827.1:n.*462C=
ENST00000642772.1:c.*94+5827C=	ENSP00000495041.1:n.*94+5827C=
ENST00000643042.1:c.511C=	ENSP00000496674.1:n.511C=
ENST00000643619.1:c.*473C=	ENSP00000494378.1:n.*473C=
ENST00000643752.1:c.*216C=	ENSP00000495000.1:n.*216C=
ENST00000644088.1:c.*211C=	ENSP00000494066.1:n.*211C=
ENST00000644591.1:c.*216C=	ENSP00000496664.1:n.*216C=
ENST00000644895.1:c.*99+5827C=	ENSP00000493872.1:n.*99+5827C=
ENST00000645345.1:c.*462C=	ENSP00000495859.1:n.*462C=
ENST00000647524.1:c.*473C=	ENSP00000495077.1:n.*473C=
ENST00000373189.5:c.890C=	ENSP00000362285.5:p.Pro297=
ENST00000469204.1:n.387C=
NM_001174098.1:c.*119C=	NP_001167569.1:n.*119C=
NM_018344.5:c.890C=	NP_060814.4:p.Pro297=
NR_033413.1:n.864C=
NR_033414.1:n.637C=
XM_006717910.2:c.656C=	XP_006717973.1:p.Pro219=
NM_001363518.1:c.656C=	NP_001350447.1:p.Pro219=
XM_017016377.2:c.452C=	XP_016871866.1:p.Pro151=
XM_017016378.2:c.272C=	XP_016871867.1:p.Pro91=
NM_018344.6:c.890C= MANE Select	NP_060814.4:p.Pro297=
NM_001174098.2:c.*119C=	NP_001167569.1:n.*119C=
NM_001363518.2:c.656C=	NP_001350447.1:p.Pro219=
NR_033413.2:n.858C=
NR_033414.2:n.631C=