Canonical Allele Identifier: CA1918678579

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362604T= , CM000672.2:g.71362604T=	GRCh38
NC_000010.10:g.73122361T= , CM000672.1:g.73122361T=	GRCh37
NC_000010.9:g.72792367T=	NCBI36
NG_017066.1:g.48352T=
NG_017066.2:g.48346T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2900T=
ENST00000373189.6:c.1424T= MANE Select	ENSP00000362285.5:p.Ile475=
ENST00000479577.2:c.1190T=	ENSP00000493995.1:p.Ile397=
ENST00000642198.1:c.*996T=	ENSP00000494827.1:n.*996T=
ENST00000642772.1:c.*94+6361T=	ENSP00000495041.1:n.*94+6361T=
ENST00000643042.1:c.1045T=	ENSP00000496674.1:n.1045T=
ENST00000643619.1:c.*1007T=	ENSP00000494378.1:n.*1007T=
ENST00000643752.1:c.*750T=	ENSP00000495000.1:n.*750T=
ENST00000644088.1:c.*745T=	ENSP00000494066.1:n.*745T=
ENST00000644591.1:c.*750T=	ENSP00000496664.1:n.*750T=
ENST00000644895.1:c.*99+6361T=	ENSP00000493872.1:n.*99+6361T=
ENST00000645345.1:c.*996T=	ENSP00000495859.1:n.*996T=
ENST00000647524.1:c.*1007T=	ENSP00000495077.1:n.*1007T=
ENST00000373189.5:c.1424T=	ENSP00000362285.5:p.Ile475=
NM_001174098.1:c.*653T=	NP_001167569.1:n.*653T=
NM_018344.5:c.1424T=	NP_060814.4:p.Ile475=
NR_033413.1:n.1398T=
NR_033414.1:n.1171T=
XM_006717910.2:c.1190T=	XP_006717973.1:p.Ile397=
NM_001363518.1:c.1190T=	NP_001350447.1:p.Ile397=
XM_017016377.2:c.986T=	XP_016871866.1:p.Ile329=
XM_017016378.2:c.806T=	XP_016871867.1:p.Ile269=
NM_018344.6:c.1424T= MANE Select	NP_060814.4:p.Ile475=
NM_001174098.2:c.*653T=	NP_001167569.1:n.*653T=
NM_001363518.2:c.1190T=	NP_001350447.1:p.Ile397=
NR_033413.2:n.1392T=
NR_033414.2:n.1165T=