Canonical Allele Identifier: CA1918678474

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362374C= , CM000672.2:g.71362374C=	GRCh38
NC_000010.10:g.73122131C= , CM000672.1:g.73122131C=	GRCh37
NC_000010.9:g.72792137C=	NCBI36
NG_017066.1:g.48122C=
NG_017066.2:g.48116C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2670C=
ENST00000373189.6:c.1194C= MANE Select	ENSP00000362285.5:p.Tyr398=
ENST00000479577.2:c.960C=	ENSP00000493995.1:p.Tyr320=
ENST00000642198.1:c.*766C=	ENSP00000494827.1:n.*766C=
ENST00000642772.1:c.*94+6131C=	ENSP00000495041.1:n.*94+6131C=
ENST00000643042.1:c.815C=	ENSP00000496674.1:n.815C=
ENST00000643619.1:c.*777C=	ENSP00000494378.1:n.*777C=
ENST00000643752.1:c.*520C=	ENSP00000495000.1:n.*520C=
ENST00000644088.1:c.*515C=	ENSP00000494066.1:n.*515C=
ENST00000644591.1:c.*520C=	ENSP00000496664.1:n.*520C=
ENST00000644895.1:c.*99+6131C=	ENSP00000493872.1:n.*99+6131C=
ENST00000645345.1:c.*766C=	ENSP00000495859.1:n.*766C=
ENST00000647524.1:c.*777C=	ENSP00000495077.1:n.*777C=
ENST00000373189.5:c.1194C=	ENSP00000362285.5:p.Tyr398=
ENST00000469204.1:n.691C=
NM_001174098.1:c.*423C=	NP_001167569.1:n.*423C=
NM_018344.5:c.1194C=	NP_060814.4:p.Tyr398=
NR_033413.1:n.1168C=
NR_033414.1:n.941C=
XM_006717910.2:c.960C=	XP_006717973.1:p.Tyr320=
NM_001363518.1:c.960C=	NP_001350447.1:p.Tyr320=
XM_017016377.2:c.756C=	XP_016871866.1:p.Tyr252=
XM_017016378.2:c.576C=	XP_016871867.1:p.Tyr192=
NM_018344.6:c.1194C= MANE Select	NP_060814.4:p.Tyr398=
NM_001174098.2:c.*423C=	NP_001167569.1:n.*423C=
NM_001363518.2:c.960C=	NP_001350447.1:p.Tyr320=
NR_033413.2:n.1162C=
NR_033414.2:n.935C=