Canonical Allele Identifier: CA470280906

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73121798C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362041C>A , CM000672.2:g.71362041C>A	GRCh38
NC_000010.10:g.73121798C>A , CM000672.1:g.73121798C>A	GRCh37
NC_000010.9:g.72791804C>A	NCBI36
NG_017066.1:g.47789C>A
NG_017066.2:g.47783C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2337C>A
ENST00000373189.6:c.861C>A MANE Select	ENSP00000362285.5:p.Ala287=
ENST00000479577.2:c.627C>A	ENSP00000493995.1:p.Ala209=
ENST00000642198.1:c.*433C>A	ENSP00000494827.1:n.*433C>A
ENST00000642772.1:c.*94+5798C>A	ENSP00000495041.1:n.*94+5798C>A
ENST00000643042.1:c.482C>A	ENSP00000496674.1:n.482C>A
ENST00000643619.1:c.*444C>A	ENSP00000494378.1:n.*444C>A
ENST00000643752.1:c.*187C>A	ENSP00000495000.1:n.*187C>A
ENST00000644088.1:c.*182C>A	ENSP00000494066.1:n.*182C>A
ENST00000644591.1:c.*187C>A	ENSP00000496664.1:n.*187C>A
ENST00000644895.1:c.*99+5798C>A	ENSP00000493872.1:n.*99+5798C>A
ENST00000645345.1:c.*433C>A	ENSP00000495859.1:n.*433C>A
ENST00000647524.1:c.*444C>A	ENSP00000495077.1:n.*444C>A
ENST00000373189.5:c.861C>A	ENSP00000362285.5:p.Ala287=
ENST00000469204.1:n.358C>A
NM_001174098.1:c.*90C>A	NP_001167569.1:n.*90C>A
NM_018344.5:c.861C>A	NP_060814.4:p.Ala287=
NR_033413.1:n.835C>A
NR_033414.1:n.608C>A
XM_006717910.2:c.627C>A	XP_006717973.1:p.Ala209=
NM_001363518.1:c.627C>A	NP_001350447.1:p.Ala209=
XM_017016377.2:c.423C>A	XP_016871866.1:p.Ala141=
XM_017016378.2:c.243C>A	XP_016871867.1:p.Ala81=
NM_018344.6:c.861C>A MANE Select	NP_060814.4:p.Ala287=
NM_001174098.2:c.*90C>A	NP_001167569.1:n.*90C>A
NM_001363518.2:c.627C>A	NP_001350447.1:p.Ala209=
NR_033413.2:n.829C>A
NR_033414.2:n.602C>A