Canonical Allele Identifier: CA1918678282

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71361966G= , CM000672.2:g.71361966G=	GRCh38
NC_000010.10:g.73121723G= , CM000672.1:g.73121723G=	GRCh37
NC_000010.9:g.72791729G=	NCBI36
NG_017066.1:g.47714G=
NG_017066.2:g.47708G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2262G=
ENST00000373189.6:c.786G= MANE Select	ENSP00000362285.5:p.Arg262=
ENST00000479577.2:c.552G=	ENSP00000493995.1:p.Arg184=
ENST00000642198.1:c.*358G=	ENSP00000494827.1:n.*358G=
ENST00000642772.1:c.*94+5723G=	ENSP00000495041.1:n.*94+5723G=
ENST00000643042.1:c.407G=	ENSP00000496674.1:n.407G=
ENST00000643619.1:c.*369G=	ENSP00000494378.1:n.*369G=
ENST00000643752.1:c.*112G=	ENSP00000495000.1:n.*112G=
ENST00000644088.1:c.*107G=	ENSP00000494066.1:n.*107G=
ENST00000644591.1:c.*112G=	ENSP00000496664.1:n.*112G=
ENST00000644895.1:c.*99+5723G=	ENSP00000493872.1:n.*99+5723G=
ENST00000645345.1:c.*358G=	ENSP00000495859.1:n.*358G=
ENST00000647524.1:c.*369G=	ENSP00000495077.1:n.*369G=
ENST00000373189.5:c.786G=	ENSP00000362285.5:p.Arg262=
ENST00000469204.1:n.283G=
NM_001174098.1:c.*15G=	NP_001167569.1:n.*15G=
NM_018344.5:c.786G=	NP_060814.4:p.Arg262=
NR_033413.1:n.760G=
NR_033414.1:n.533G=
XM_006717910.2:c.552G=	XP_006717973.1:p.Arg184=
NM_001363518.1:c.552G=	NP_001350447.1:p.Arg184=
XM_017016377.2:c.348G=	XP_016871866.1:p.Arg116=
XM_017016378.2:c.168G=	XP_016871867.1:p.Arg56=
NM_018344.6:c.786G= MANE Select	NP_060814.4:p.Arg262=
NM_001174098.2:c.*15G=	NP_001167569.1:n.*15G=
NM_001363518.2:c.552G=	NP_001350447.1:p.Arg184=
NR_033413.2:n.754G=
NR_033414.2:n.527G=