Canonical Allele Identifier: CA1918678290

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71361979G= , CM000672.2:g.71361979G=	GRCh38
NC_000010.10:g.73121736G= , CM000672.1:g.73121736G=	GRCh37
NC_000010.9:g.72791742G=	NCBI36
NG_017066.1:g.47727G=
NG_017066.2:g.47721G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2275G=
ENST00000373189.6:c.799G= MANE Select	ENSP00000362285.5:p.Ala267=
ENST00000479577.2:c.565G=	ENSP00000493995.1:p.Ala189=
ENST00000642198.1:c.*371G=	ENSP00000494827.1:n.*371G=
ENST00000642772.1:c.*94+5736G=	ENSP00000495041.1:n.*94+5736G=
ENST00000643042.1:c.420G=	ENSP00000496674.1:n.420G=
ENST00000643619.1:c.*382G=	ENSP00000494378.1:n.*382G=
ENST00000643752.1:c.*125G=	ENSP00000495000.1:n.*125G=
ENST00000644088.1:c.*120G=	ENSP00000494066.1:n.*120G=
ENST00000644591.1:c.*125G=	ENSP00000496664.1:n.*125G=
ENST00000644895.1:c.*99+5736G=	ENSP00000493872.1:n.*99+5736G=
ENST00000645345.1:c.*371G=	ENSP00000495859.1:n.*371G=
ENST00000647524.1:c.*382G=	ENSP00000495077.1:n.*382G=
ENST00000373189.5:c.799G=	ENSP00000362285.5:p.Ala267=
ENST00000469204.1:n.296G=
NM_001174098.1:c.*28G=	NP_001167569.1:n.*28G=
NM_018344.5:c.799G=	NP_060814.4:p.Ala267=
NR_033413.1:n.773G=
NR_033414.1:n.546G=
XM_006717910.2:c.565G=	XP_006717973.1:p.Ala189=
NM_001363518.1:c.565G=	NP_001350447.1:p.Ala189=
XM_017016377.2:c.361G=	XP_016871866.1:p.Ala121=
XM_017016378.2:c.181G=	XP_016871867.1:p.Ala61=
NM_018344.6:c.799G= MANE Select	NP_060814.4:p.Ala267=
NM_001174098.2:c.*28G=	NP_001167569.1:n.*28G=
NM_001363518.2:c.565G=	NP_001350447.1:p.Ala189=
NR_033413.2:n.767G=
NR_033414.2:n.540G=