Canonical Allele Identifier: CA1918678329

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362067C= , CM000672.2:g.71362067C=	GRCh38
NC_000010.10:g.73121824C= , CM000672.1:g.73121824C=	GRCh37
NC_000010.9:g.72791830C=	NCBI36
NG_017066.1:g.47815C=
NG_017066.2:g.47809C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2363C=
ENST00000373189.6:c.887C= MANE Select	ENSP00000362285.5:p.Pro296=
ENST00000479577.2:c.653C=	ENSP00000493995.1:p.Pro218=
ENST00000642198.1:c.*459C=	ENSP00000494827.1:n.*459C=
ENST00000642772.1:c.*94+5824C=	ENSP00000495041.1:n.*94+5824C=
ENST00000643042.1:c.508C=	ENSP00000496674.1:n.508C=
ENST00000643619.1:c.*470C=	ENSP00000494378.1:n.*470C=
ENST00000643752.1:c.*213C=	ENSP00000495000.1:n.*213C=
ENST00000644088.1:c.*208C=	ENSP00000494066.1:n.*208C=
ENST00000644591.1:c.*213C=	ENSP00000496664.1:n.*213C=
ENST00000644895.1:c.*99+5824C=	ENSP00000493872.1:n.*99+5824C=
ENST00000645345.1:c.*459C=	ENSP00000495859.1:n.*459C=
ENST00000647524.1:c.*470C=	ENSP00000495077.1:n.*470C=
ENST00000373189.5:c.887C=	ENSP00000362285.5:p.Pro296=
ENST00000469204.1:n.384C=
NM_001174098.1:c.*116C=	NP_001167569.1:n.*116C=
NM_018344.5:c.887C=	NP_060814.4:p.Pro296=
NR_033413.1:n.861C=
NR_033414.1:n.634C=
XM_006717910.2:c.653C=	XP_006717973.1:p.Pro218=
NM_001363518.1:c.653C=	NP_001350447.1:p.Pro218=
XM_017016377.2:c.449C=	XP_016871866.1:p.Pro150=
XM_017016378.2:c.269C=	XP_016871867.1:p.Pro90=
NM_018344.6:c.887C= MANE Select	NP_060814.4:p.Pro296=
NM_001174098.2:c.*116C=	NP_001167569.1:n.*116C=
NM_001363518.2:c.653C=	NP_001350447.1:p.Pro218=
NR_033413.2:n.855C=
NR_033414.2:n.628C=