Canonical Allele Identifier: CA1918678296

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71361997G= , CM000672.2:g.71361997G=	GRCh38
NC_000010.10:g.73121754G= , CM000672.1:g.73121754G=	GRCh37
NC_000010.9:g.72791760G=	NCBI36
NG_017066.1:g.47745G=
NG_017066.2:g.47739G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2293G=
ENST00000373189.6:c.817G= MANE Select	ENSP00000362285.5:p.Glu273=
ENST00000479577.2:c.583G=	ENSP00000493995.1:p.Glu195=
ENST00000642198.1:c.*389G=	ENSP00000494827.1:n.*389G=
ENST00000642772.1:c.*94+5754G=	ENSP00000495041.1:n.*94+5754G=
ENST00000643042.1:c.438G=	ENSP00000496674.1:n.438G=
ENST00000643619.1:c.*400G=	ENSP00000494378.1:n.*400G=
ENST00000643752.1:c.*143G=	ENSP00000495000.1:n.*143G=
ENST00000644088.1:c.*138G=	ENSP00000494066.1:n.*138G=
ENST00000644591.1:c.*143G=	ENSP00000496664.1:n.*143G=
ENST00000644895.1:c.*99+5754G=	ENSP00000493872.1:n.*99+5754G=
ENST00000645345.1:c.*389G=	ENSP00000495859.1:n.*389G=
ENST00000647524.1:c.*400G=	ENSP00000495077.1:n.*400G=
ENST00000373189.5:c.817G=	ENSP00000362285.5:p.Glu273=
ENST00000469204.1:n.314G=
NM_001174098.1:c.*46G=	NP_001167569.1:n.*46G=
NM_018344.5:c.817G=	NP_060814.4:p.Glu273=
NR_033413.1:n.791G=
NR_033414.1:n.564G=
XM_006717910.2:c.583G=	XP_006717973.1:p.Glu195=
NM_001363518.1:c.583G=	NP_001350447.1:p.Glu195=
XM_017016377.2:c.379G=	XP_016871866.1:p.Glu127=
XM_017016378.2:c.199G=	XP_016871867.1:p.Glu67=
NM_018344.6:c.817G= MANE Select	NP_060814.4:p.Glu273=
NM_001174098.2:c.*46G=	NP_001167569.1:n.*46G=
NM_001363518.2:c.583G=	NP_001350447.1:p.Glu195=
NR_033413.2:n.785G=
NR_033414.2:n.558G=