Canonical Allele Identifier: CA1918678395

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362188T= , CM000672.2:g.71362188T=	GRCh38
NC_000010.10:g.73121945T= , CM000672.1:g.73121945T=	GRCh37
NC_000010.9:g.72791951T=	NCBI36
NG_017066.1:g.47936T=
NG_017066.2:g.47930T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000697843.1:n.2484T=
ENST00000373189.6:c.1008T= MANE Select	ENSP00000362285.5:p.Gly336=
ENST00000479577.2:c.774T=	ENSP00000493995.1:p.Gly258=
ENST00000642198.1:c.*580T=	ENSP00000494827.1:n.*580T=
ENST00000642772.1:c.*94+5945T=	ENSP00000495041.1:n.*94+5945T=
ENST00000643042.1:c.629T=	ENSP00000496674.1:n.629T=
ENST00000643619.1:c.*591T=	ENSP00000494378.1:n.*591T=
ENST00000643752.1:c.*334T=	ENSP00000495000.1:n.*334T=
ENST00000644088.1:c.*329T=	ENSP00000494066.1:n.*329T=
ENST00000644591.1:c.*334T=	ENSP00000496664.1:n.*334T=
ENST00000644895.1:c.*99+5945T=	ENSP00000493872.1:n.*99+5945T=
ENST00000645345.1:c.*580T=	ENSP00000495859.1:n.*580T=
ENST00000647524.1:c.*591T=	ENSP00000495077.1:n.*591T=
ENST00000373189.5:c.1008T=	ENSP00000362285.5:p.Gly336=
ENST00000469204.1:n.505T=
NM_001174098.1:c.*237T=	NP_001167569.1:n.*237T=
NM_018344.5:c.1008T=	NP_060814.4:p.Gly336=
NR_033413.1:n.982T=
NR_033414.1:n.755T=
XM_006717910.2:c.774T=	XP_006717973.1:p.Gly258=
NM_001363518.1:c.774T=	NP_001350447.1:p.Gly258=
XM_017016377.2:c.570T=	XP_016871866.1:p.Gly190=
XM_017016378.2:c.390T=	XP_016871867.1:p.Gly130=
NM_018344.6:c.1008T= MANE Select	NP_060814.4:p.Gly336=
NM_001174098.2:c.*237T=	NP_001167569.1:n.*237T=
NM_001363518.2:c.774T=	NP_001350447.1:p.Gly258=
NR_033413.2:n.976T=
NR_033414.2:n.749T=