Canonical Allele Identifier: CA1918678492

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362409A= , CM000672.2:g.71362409A=	GRCh38
NC_000010.10:g.73122166A= , CM000672.1:g.73122166A=	GRCh37
NC_000010.9:g.72792172A=	NCBI36
NG_017066.1:g.48157A=
NG_017066.2:g.48151A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2705A=
ENST00000373189.6:c.1229A= MANE Select	ENSP00000362285.5:p.Gln410=
ENST00000479577.2:c.995A=	ENSP00000493995.1:p.Gln332=
ENST00000642198.1:c.*801A=	ENSP00000494827.1:n.*801A=
ENST00000642772.1:c.*94+6166A=	ENSP00000495041.1:n.*94+6166A=
ENST00000643042.1:c.850A=	ENSP00000496674.1:n.850A=
ENST00000643619.1:c.*812A=	ENSP00000494378.1:n.*812A=
ENST00000643752.1:c.*555A=	ENSP00000495000.1:n.*555A=
ENST00000644088.1:c.*550A=	ENSP00000494066.1:n.*550A=
ENST00000644591.1:c.*555A=	ENSP00000496664.1:n.*555A=
ENST00000644895.1:c.*99+6166A=	ENSP00000493872.1:n.*99+6166A=
ENST00000645345.1:c.*801A=	ENSP00000495859.1:n.*801A=
ENST00000647524.1:c.*812A=	ENSP00000495077.1:n.*812A=
ENST00000373189.5:c.1229A=	ENSP00000362285.5:p.Gln410=
ENST00000469204.1:n.726A=
NM_001174098.1:c.*458A=	NP_001167569.1:n.*458A=
NM_018344.5:c.1229A=	NP_060814.4:p.Gln410=
NR_033413.1:n.1203A=
NR_033414.1:n.976A=
XM_006717910.2:c.995A=	XP_006717973.1:p.Gln332=
NM_001363518.1:c.995A=	NP_001350447.1:p.Gln332=
XM_017016377.2:c.791A=	XP_016871866.1:p.Gln264=
XM_017016378.2:c.611A=	XP_016871867.1:p.Gln204=
NM_018344.6:c.1229A= MANE Select	NP_060814.4:p.Gln410=
NM_001174098.2:c.*458A=	NP_001167569.1:n.*458A=
NM_001363518.2:c.995A=	NP_001350447.1:p.Gln332=
NR_033413.2:n.1197A=
NR_033414.2:n.970A=