Canonical Allele Identifier: CA1918678317

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362041C= , CM000672.2:g.71362041C=	GRCh38
NC_000010.10:g.73121798C= , CM000672.1:g.73121798C=	GRCh37
NC_000010.9:g.72791804C=	NCBI36
NG_017066.1:g.47789C=
NG_017066.2:g.47783C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2337C=
ENST00000373189.6:c.861C= MANE Select	ENSP00000362285.5:p.Ala287=
ENST00000479577.2:c.627C=	ENSP00000493995.1:p.Ala209=
ENST00000642198.1:c.*433C=	ENSP00000494827.1:n.*433C=
ENST00000642772.1:c.*94+5798C=	ENSP00000495041.1:n.*94+5798C=
ENST00000643042.1:c.482C=	ENSP00000496674.1:n.482C=
ENST00000643619.1:c.*444C=	ENSP00000494378.1:n.*444C=
ENST00000643752.1:c.*187C=	ENSP00000495000.1:n.*187C=
ENST00000644088.1:c.*182C=	ENSP00000494066.1:n.*182C=
ENST00000644591.1:c.*187C=	ENSP00000496664.1:n.*187C=
ENST00000644895.1:c.*99+5798C=	ENSP00000493872.1:n.*99+5798C=
ENST00000645345.1:c.*433C=	ENSP00000495859.1:n.*433C=
ENST00000647524.1:c.*444C=	ENSP00000495077.1:n.*444C=
ENST00000373189.5:c.861C=	ENSP00000362285.5:p.Ala287=
ENST00000469204.1:n.358C=
NM_001174098.1:c.*90C=	NP_001167569.1:n.*90C=
NM_018344.5:c.861C=	NP_060814.4:p.Ala287=
NR_033413.1:n.835C=
NR_033414.1:n.608C=
XM_006717910.2:c.627C=	XP_006717973.1:p.Ala209=
NM_001363518.1:c.627C=	NP_001350447.1:p.Ala209=
XM_017016377.2:c.423C=	XP_016871866.1:p.Ala141=
XM_017016378.2:c.243C=	XP_016871867.1:p.Ala81=
NM_018344.6:c.861C= MANE Select	NP_060814.4:p.Ala287=
NM_001174098.2:c.*90C=	NP_001167569.1:n.*90C=
NM_001363518.2:c.627C=	NP_001350447.1:p.Ala209=
NR_033413.2:n.829C=
NR_033414.2:n.602C=