Canonical Allele Identifier: CA1918678318

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362042T= , CM000672.2:g.71362042T=	GRCh38
NC_000010.10:g.73121799T= , CM000672.1:g.73121799T=	GRCh37
NC_000010.9:g.72791805T=	NCBI36
NG_017066.1:g.47790T=
NG_017066.2:g.47784T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2338T=
ENST00000373189.6:c.862T= MANE Select	ENSP00000362285.5:p.Ser288=
ENST00000479577.2:c.628T=	ENSP00000493995.1:p.Ser210=
ENST00000642198.1:c.*434T=	ENSP00000494827.1:n.*434T=
ENST00000642772.1:c.*94+5799T=	ENSP00000495041.1:n.*94+5799T=
ENST00000643042.1:c.483T=	ENSP00000496674.1:n.483T=
ENST00000643619.1:c.*445T=	ENSP00000494378.1:n.*445T=
ENST00000643752.1:c.*188T=	ENSP00000495000.1:n.*188T=
ENST00000644088.1:c.*183T=	ENSP00000494066.1:n.*183T=
ENST00000644591.1:c.*188T=	ENSP00000496664.1:n.*188T=
ENST00000644895.1:c.*99+5799T=	ENSP00000493872.1:n.*99+5799T=
ENST00000645345.1:c.*434T=	ENSP00000495859.1:n.*434T=
ENST00000647524.1:c.*445T=	ENSP00000495077.1:n.*445T=
ENST00000373189.5:c.862T=	ENSP00000362285.5:p.Ser288=
ENST00000469204.1:n.359T=
NM_001174098.1:c.*91T=	NP_001167569.1:n.*91T=
NM_018344.5:c.862T=	NP_060814.4:p.Ser288=
NR_033413.1:n.836T=
NR_033414.1:n.609T=
XM_006717910.2:c.628T=	XP_006717973.1:p.Ser210=
NM_001363518.1:c.628T=	NP_001350447.1:p.Ser210=
XM_017016377.2:c.424T=	XP_016871866.1:p.Ser142=
XM_017016378.2:c.244T=	XP_016871867.1:p.Ser82=
NM_018344.6:c.862T= MANE Select	NP_060814.4:p.Ser288=
NM_001174098.2:c.*91T=	NP_001167569.1:n.*91T=
NM_001363518.2:c.628T=	NP_001350447.1:p.Ser210=
NR_033413.2:n.830T=
NR_033414.2:n.603T=