Canonical Allele Identifier: CA1918678368

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362147T= , CM000672.2:g.71362147T=	GRCh38
NC_000010.10:g.73121904T= , CM000672.1:g.73121904T=	GRCh37
NC_000010.9:g.72791910T=	NCBI36
NG_017066.1:g.47895T=
NG_017066.2:g.47889T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2443T=
ENST00000373189.6:c.967T= MANE Select	ENSP00000362285.5:p.Tyr323=
ENST00000479577.2:c.733T=	ENSP00000493995.1:p.Tyr245=
ENST00000642198.1:c.*539T=	ENSP00000494827.1:n.*539T=
ENST00000642772.1:c.*94+5904T=	ENSP00000495041.1:n.*94+5904T=
ENST00000643042.1:c.588T=	ENSP00000496674.1:n.588T=
ENST00000643619.1:c.*550T=	ENSP00000494378.1:n.*550T=
ENST00000643752.1:c.*293T=	ENSP00000495000.1:n.*293T=
ENST00000644088.1:c.*288T=	ENSP00000494066.1:n.*288T=
ENST00000644591.1:c.*293T=	ENSP00000496664.1:n.*293T=
ENST00000644895.1:c.*99+5904T=	ENSP00000493872.1:n.*99+5904T=
ENST00000645345.1:c.*539T=	ENSP00000495859.1:n.*539T=
ENST00000647524.1:c.*550T=	ENSP00000495077.1:n.*550T=
ENST00000373189.5:c.967T=	ENSP00000362285.5:p.Tyr323=
ENST00000469204.1:n.464T=
NM_001174098.1:c.*196T=	NP_001167569.1:n.*196T=
NM_018344.5:c.967T=	NP_060814.4:p.Tyr323=
NR_033413.1:n.941T=
NR_033414.1:n.714T=
XM_006717910.2:c.733T=	XP_006717973.1:p.Tyr245=
NM_001363518.1:c.733T=	NP_001350447.1:p.Tyr245=
XM_017016377.2:c.529T=	XP_016871866.1:p.Tyr177=
XM_017016378.2:c.349T=	XP_016871867.1:p.Tyr117=
NM_018344.6:c.967T= MANE Select	NP_060814.4:p.Tyr323=
NM_001174098.2:c.*196T=	NP_001167569.1:n.*196T=
NM_001363518.2:c.733T=	NP_001350447.1:p.Tyr245=
NR_033413.2:n.935T=
NR_033414.2:n.708T=