Canonical Allele Identifier: CA1918678400

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362196C= , CM000672.2:g.71362196C=	GRCh38
NC_000010.10:g.73121953C= , CM000672.1:g.73121953C=	GRCh37
NC_000010.9:g.72791959C=	NCBI36
NG_017066.1:g.47944C=
NG_017066.2:g.47938C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000697843.1:n.2492C=
ENST00000373189.6:c.1016C= MANE Select	ENSP00000362285.5:p.Ser339=
ENST00000479577.2:c.782C=	ENSP00000493995.1:p.Ser261=
ENST00000642198.1:c.*588C=	ENSP00000494827.1:n.*588C=
ENST00000642772.1:c.*94+5953C=	ENSP00000495041.1:n.*94+5953C=
ENST00000643042.1:c.637C=	ENSP00000496674.1:n.637C=
ENST00000643619.1:c.*599C=	ENSP00000494378.1:n.*599C=
ENST00000643752.1:c.*342C=	ENSP00000495000.1:n.*342C=
ENST00000644088.1:c.*337C=	ENSP00000494066.1:n.*337C=
ENST00000644591.1:c.*342C=	ENSP00000496664.1:n.*342C=
ENST00000644895.1:c.*99+5953C=	ENSP00000493872.1:n.*99+5953C=
ENST00000645345.1:c.*588C=	ENSP00000495859.1:n.*588C=
ENST00000647524.1:c.*599C=	ENSP00000495077.1:n.*599C=
ENST00000373189.5:c.1016C=	ENSP00000362285.5:p.Ser339=
ENST00000469204.1:n.513C=
NM_001174098.1:c.*245C=	NP_001167569.1:n.*245C=
NM_018344.5:c.1016C=	NP_060814.4:p.Ser339=
NR_033413.1:n.990C=
NR_033414.1:n.763C=
XM_006717910.2:c.782C=	XP_006717973.1:p.Ser261=
NM_001363518.1:c.782C=	NP_001350447.1:p.Ser261=
XM_017016377.2:c.578C=	XP_016871866.1:p.Ser193=
XM_017016378.2:c.398C=	XP_016871867.1:p.Ser133=
NM_018344.6:c.1016C= MANE Select	NP_060814.4:p.Ser339=
NM_001174098.2:c.*245C=	NP_001167569.1:n.*245C=
NM_001363518.2:c.782C=	NP_001350447.1:p.Ser261=
NR_033413.2:n.984C=
NR_033414.2:n.757C=