Canonical Allele Identifier: CA1918678493

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362410G= , CM000672.2:g.71362410G=	GRCh38
NC_000010.10:g.73122167G= , CM000672.1:g.73122167G=	GRCh37
NC_000010.9:g.72792173G=	NCBI36
NG_017066.1:g.48158G=
NG_017066.2:g.48152G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2706G=
ENST00000373189.6:c.1230G= MANE Select	ENSP00000362285.5:p.Gln410=
ENST00000479577.2:c.996G=	ENSP00000493995.1:p.Gln332=
ENST00000642198.1:c.*802G=	ENSP00000494827.1:n.*802G=
ENST00000642772.1:c.*94+6167G=	ENSP00000495041.1:n.*94+6167G=
ENST00000643042.1:c.851G=	ENSP00000496674.1:n.851G=
ENST00000643619.1:c.*813G=	ENSP00000494378.1:n.*813G=
ENST00000643752.1:c.*556G=	ENSP00000495000.1:n.*556G=
ENST00000644088.1:c.*551G=	ENSP00000494066.1:n.*551G=
ENST00000644591.1:c.*556G=	ENSP00000496664.1:n.*556G=
ENST00000644895.1:c.*99+6167G=	ENSP00000493872.1:n.*99+6167G=
ENST00000645345.1:c.*802G=	ENSP00000495859.1:n.*802G=
ENST00000647524.1:c.*813G=	ENSP00000495077.1:n.*813G=
ENST00000373189.5:c.1230G=	ENSP00000362285.5:p.Gln410=
ENST00000469204.1:n.727G=
NM_001174098.1:c.*459G=	NP_001167569.1:n.*459G=
NM_018344.5:c.1230G=	NP_060814.4:p.Gln410=
NR_033413.1:n.1204G=
NR_033414.1:n.977G=
XM_006717910.2:c.996G=	XP_006717973.1:p.Gln332=
NM_001363518.1:c.996G=	NP_001350447.1:p.Gln332=
XM_017016377.2:c.792G=	XP_016871866.1:p.Gln264=
XM_017016378.2:c.612G=	XP_016871867.1:p.Gln204=
NM_018344.6:c.1230G= MANE Select	NP_060814.4:p.Gln410=
NM_001174098.2:c.*459G=	NP_001167569.1:n.*459G=
NM_001363518.2:c.996G=	NP_001350447.1:p.Gln332=
NR_033413.2:n.1198G=
NR_033414.2:n.971G=