Canonical Allele Identifier: CA1918678350

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362105G= , CM000672.2:g.71362105G=	GRCh38
NC_000010.10:g.73121862G= , CM000672.1:g.73121862G=	GRCh37
NC_000010.9:g.72791868G=	NCBI36
NG_017066.1:g.47853G=
NG_017066.2:g.47847G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2401G=
ENST00000373189.6:c.925G= MANE Select	ENSP00000362285.5:p.Gly309=
ENST00000479577.2:c.691G=	ENSP00000493995.1:p.Gly231=
ENST00000642198.1:c.*497G=	ENSP00000494827.1:n.*497G=
ENST00000642772.1:c.*94+5862G=	ENSP00000495041.1:n.*94+5862G=
ENST00000643042.1:c.546G=	ENSP00000496674.1:n.546G=
ENST00000643619.1:c.*508G=	ENSP00000494378.1:n.*508G=
ENST00000643752.1:c.*251G=	ENSP00000495000.1:n.*251G=
ENST00000644088.1:c.*246G=	ENSP00000494066.1:n.*246G=
ENST00000644591.1:c.*251G=	ENSP00000496664.1:n.*251G=
ENST00000644895.1:c.*99+5862G=	ENSP00000493872.1:n.*99+5862G=
ENST00000645345.1:c.*497G=	ENSP00000495859.1:n.*497G=
ENST00000647524.1:c.*508G=	ENSP00000495077.1:n.*508G=
ENST00000373189.5:c.925G=	ENSP00000362285.5:p.Gly309=
ENST00000469204.1:n.422G=
NM_001174098.1:c.*154G=	NP_001167569.1:n.*154G=
NM_018344.5:c.925G=	NP_060814.4:p.Gly309=
NR_033413.1:n.899G=
NR_033414.1:n.672G=
XM_006717910.2:c.691G=	XP_006717973.1:p.Gly231=
NM_001363518.1:c.691G=	NP_001350447.1:p.Gly231=
XM_017016377.2:c.487G=	XP_016871866.1:p.Gly163=
XM_017016378.2:c.307G=	XP_016871867.1:p.Gly103=
NM_018344.6:c.925G= MANE Select	NP_060814.4:p.Gly309=
NM_001174098.2:c.*154G=	NP_001167569.1:n.*154G=
NM_001363518.2:c.691G=	NP_001350447.1:p.Gly231=
NR_033413.2:n.893G=
NR_033414.2:n.666G=