Canonical Allele Identifier: CA1918678285

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71361971T= , CM000672.2:g.71361971T=	GRCh38
NC_000010.10:g.73121728T= , CM000672.1:g.73121728T=	GRCh37
NC_000010.9:g.72791734T=	NCBI36
NG_017066.1:g.47719T=
NG_017066.2:g.47713T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2267T=
ENST00000373189.6:c.791T= MANE Select	ENSP00000362285.5:p.Val264=
ENST00000479577.2:c.557T=	ENSP00000493995.1:p.Val186=
ENST00000642198.1:c.*363T=	ENSP00000494827.1:n.*363T=
ENST00000642772.1:c.*94+5728T=	ENSP00000495041.1:n.*94+5728T=
ENST00000643042.1:c.412T=	ENSP00000496674.1:n.412T=
ENST00000643619.1:c.*374T=	ENSP00000494378.1:n.*374T=
ENST00000643752.1:c.*117T=	ENSP00000495000.1:n.*117T=
ENST00000644088.1:c.*112T=	ENSP00000494066.1:n.*112T=
ENST00000644591.1:c.*117T=	ENSP00000496664.1:n.*117T=
ENST00000644895.1:c.*99+5728T=	ENSP00000493872.1:n.*99+5728T=
ENST00000645345.1:c.*363T=	ENSP00000495859.1:n.*363T=
ENST00000647524.1:c.*374T=	ENSP00000495077.1:n.*374T=
ENST00000373189.5:c.791T=	ENSP00000362285.5:p.Val264=
ENST00000469204.1:n.288T=
NM_001174098.1:c.*20T=	NP_001167569.1:n.*20T=
NM_018344.5:c.791T=	NP_060814.4:p.Val264=
NR_033413.1:n.765T=
NR_033414.1:n.538T=
XM_006717910.2:c.557T=	XP_006717973.1:p.Val186=
NM_001363518.1:c.557T=	NP_001350447.1:p.Val186=
XM_017016377.2:c.353T=	XP_016871866.1:p.Val118=
XM_017016378.2:c.173T=	XP_016871867.1:p.Val58=
NM_018344.6:c.791T= MANE Select	NP_060814.4:p.Val264=
NM_001174098.2:c.*20T=	NP_001167569.1:n.*20T=
NM_001363518.2:c.557T=	NP_001350447.1:p.Val186=
NR_033413.2:n.759T=
NR_033414.2:n.532T=