Canonical Allele Identifier: CA1918678461

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362348A= , CM000672.2:g.71362348A=	GRCh38
NC_000010.10:g.73122105A= , CM000672.1:g.73122105A=	GRCh37
NC_000010.9:g.72792111A=	NCBI36
NG_017066.1:g.48096A=
NG_017066.2:g.48090A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2644A=
ENST00000373189.6:c.1168A= MANE Select	ENSP00000362285.5:p.Ile390=
ENST00000479577.2:c.934A=	ENSP00000493995.1:p.Ile312=
ENST00000642198.1:c.*740A=	ENSP00000494827.1:n.*740A=
ENST00000642772.1:c.*94+6105A=	ENSP00000495041.1:n.*94+6105A=
ENST00000643042.1:c.789A=	ENSP00000496674.1:n.789A=
ENST00000643619.1:c.*751A=	ENSP00000494378.1:n.*751A=
ENST00000643752.1:c.*494A=	ENSP00000495000.1:n.*494A=
ENST00000644088.1:c.*489A=	ENSP00000494066.1:n.*489A=
ENST00000644591.1:c.*494A=	ENSP00000496664.1:n.*494A=
ENST00000644895.1:c.*99+6105A=	ENSP00000493872.1:n.*99+6105A=
ENST00000645345.1:c.*740A=	ENSP00000495859.1:n.*740A=
ENST00000647524.1:c.*751A=	ENSP00000495077.1:n.*751A=
ENST00000373189.5:c.1168A=	ENSP00000362285.5:p.Ile390=
ENST00000469204.1:n.665A=
NM_001174098.1:c.*397A=	NP_001167569.1:n.*397A=
NM_018344.5:c.1168A=	NP_060814.4:p.Ile390=
NR_033413.1:n.1142A=
NR_033414.1:n.915A=
XM_006717910.2:c.934A=	XP_006717973.1:p.Ile312=
NM_001363518.1:c.934A=	NP_001350447.1:p.Ile312=
XM_017016377.2:c.730A=	XP_016871866.1:p.Ile244=
XM_017016378.2:c.550A=	XP_016871867.1:p.Ile184=
NM_018344.6:c.1168A= MANE Select	NP_060814.4:p.Ile390=
NM_001174098.2:c.*397A=	NP_001167569.1:n.*397A=
NM_001363518.2:c.934A=	NP_001350447.1:p.Ile312=
NR_033413.2:n.1136A=
NR_033414.2:n.909A=