Canonical Allele Identifier: CA1918678323

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362054G= , CM000672.2:g.71362054G=	GRCh38
NC_000010.10:g.73121811G= , CM000672.1:g.73121811G=	GRCh37
NC_000010.9:g.72791817G=	NCBI36
NG_017066.1:g.47802G=
NG_017066.2:g.47796G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2350G=
ENST00000373189.6:c.874G= MANE Select	ENSP00000362285.5:p.Asp292=
ENST00000479577.2:c.640G=	ENSP00000493995.1:p.Asp214=
ENST00000642198.1:c.*446G=	ENSP00000494827.1:n.*446G=
ENST00000642772.1:c.*94+5811G=	ENSP00000495041.1:n.*94+5811G=
ENST00000643042.1:c.495G=	ENSP00000496674.1:n.495G=
ENST00000643619.1:c.*457G=	ENSP00000494378.1:n.*457G=
ENST00000643752.1:c.*200G=	ENSP00000495000.1:n.*200G=
ENST00000644088.1:c.*195G=	ENSP00000494066.1:n.*195G=
ENST00000644591.1:c.*200G=	ENSP00000496664.1:n.*200G=
ENST00000644895.1:c.*99+5811G=	ENSP00000493872.1:n.*99+5811G=
ENST00000645345.1:c.*446G=	ENSP00000495859.1:n.*446G=
ENST00000647524.1:c.*457G=	ENSP00000495077.1:n.*457G=
ENST00000373189.5:c.874G=	ENSP00000362285.5:p.Asp292=
ENST00000469204.1:n.371G=
NM_001174098.1:c.*103G=	NP_001167569.1:n.*103G=
NM_018344.5:c.874G=	NP_060814.4:p.Asp292=
NR_033413.1:n.848G=
NR_033414.1:n.621G=
XM_006717910.2:c.640G=	XP_006717973.1:p.Asp214=
NM_001363518.1:c.640G=	NP_001350447.1:p.Asp214=
XM_017016377.2:c.436G=	XP_016871866.1:p.Asp146=
XM_017016378.2:c.256G=	XP_016871867.1:p.Asp86=
NM_018344.6:c.874G= MANE Select	NP_060814.4:p.Asp292=
NM_001174098.2:c.*103G=	NP_001167569.1:n.*103G=
NM_001363518.2:c.640G=	NP_001350447.1:p.Asp214=
NR_033413.2:n.842G=
NR_033414.2:n.615G=