Canonical Allele Identifier: CA1918678304

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362019C= , CM000672.2:g.71362019C=	GRCh38
NC_000010.10:g.73121776C= , CM000672.1:g.73121776C=	GRCh37
NC_000010.9:g.72791782C=	NCBI36
NG_017066.1:g.47767C=
NG_017066.2:g.47761C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2315C=
ENST00000373189.6:c.839C= MANE Select	ENSP00000362285.5:p.Ser280=
ENST00000479577.2:c.605C=	ENSP00000493995.1:p.Ser202=
ENST00000642198.1:c.*411C=	ENSP00000494827.1:n.*411C=
ENST00000642772.1:c.*94+5776C=	ENSP00000495041.1:n.*94+5776C=
ENST00000643042.1:c.460C=	ENSP00000496674.1:n.460C=
ENST00000643619.1:c.*422C=	ENSP00000494378.1:n.*422C=
ENST00000643752.1:c.*165C=	ENSP00000495000.1:n.*165C=
ENST00000644088.1:c.*160C=	ENSP00000494066.1:n.*160C=
ENST00000644591.1:c.*165C=	ENSP00000496664.1:n.*165C=
ENST00000644895.1:c.*99+5776C=	ENSP00000493872.1:n.*99+5776C=
ENST00000645345.1:c.*411C=	ENSP00000495859.1:n.*411C=
ENST00000647524.1:c.*422C=	ENSP00000495077.1:n.*422C=
ENST00000373189.5:c.839C=	ENSP00000362285.5:p.Ser280=
ENST00000469204.1:n.336C=
NM_001174098.1:c.*68C=	NP_001167569.1:n.*68C=
NM_018344.5:c.839C=	NP_060814.4:p.Ser280=
NR_033413.1:n.813C=
NR_033414.1:n.586C=
XM_006717910.2:c.605C=	XP_006717973.1:p.Ser202=
NM_001363518.1:c.605C=	NP_001350447.1:p.Ser202=
XM_017016377.2:c.401C=	XP_016871866.1:p.Ser134=
XM_017016378.2:c.221C=	XP_016871867.1:p.Ser74=
NM_018344.6:c.839C= MANE Select	NP_060814.4:p.Ser280=
NM_001174098.2:c.*68C=	NP_001167569.1:n.*68C=
NM_001363518.2:c.605C=	NP_001350447.1:p.Ser202=
NR_033413.2:n.807C=
NR_033414.2:n.580C=