Canonical Allele Identifier: CA1918678496

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362413C= , CM000672.2:g.71362413C=	GRCh38
NC_000010.10:g.73122170C= , CM000672.1:g.73122170C=	GRCh37
NC_000010.9:g.72792176C=	NCBI36
NG_017066.1:g.48161C=
NG_017066.2:g.48155C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2709C=
ENST00000373189.6:c.1233C= MANE Select	ENSP00000362285.5:p.Ser411=
ENST00000479577.2:c.999C=	ENSP00000493995.1:p.Ser333=
ENST00000642198.1:c.*805C=	ENSP00000494827.1:n.*805C=
ENST00000642772.1:c.*94+6170C=	ENSP00000495041.1:n.*94+6170C=
ENST00000643042.1:c.854C=	ENSP00000496674.1:n.854C=
ENST00000643619.1:c.*816C=	ENSP00000494378.1:n.*816C=
ENST00000643752.1:c.*559C=	ENSP00000495000.1:n.*559C=
ENST00000644088.1:c.*554C=	ENSP00000494066.1:n.*554C=
ENST00000644591.1:c.*559C=	ENSP00000496664.1:n.*559C=
ENST00000644895.1:c.*99+6170C=	ENSP00000493872.1:n.*99+6170C=
ENST00000645345.1:c.*805C=	ENSP00000495859.1:n.*805C=
ENST00000647524.1:c.*816C=	ENSP00000495077.1:n.*816C=
ENST00000373189.5:c.1233C=	ENSP00000362285.5:p.Ser411=
ENST00000469204.1:n.730C=
NM_001174098.1:c.*462C=	NP_001167569.1:n.*462C=
NM_018344.5:c.1233C=	NP_060814.4:p.Ser411=
NR_033413.1:n.1207C=
NR_033414.1:n.980C=
XM_006717910.2:c.999C=	XP_006717973.1:p.Ser333=
NM_001363518.1:c.999C=	NP_001350447.1:p.Ser333=
XM_017016377.2:c.795C=	XP_016871866.1:p.Ser265=
XM_017016378.2:c.615C=	XP_016871867.1:p.Ser205=
NM_018344.6:c.1233C= MANE Select	NP_060814.4:p.Ser411=
NM_001174098.2:c.*462C=	NP_001167569.1:n.*462C=
NM_001363518.2:c.999C=	NP_001350447.1:p.Ser333=
NR_033413.2:n.1201C=
NR_033414.2:n.974C=