Canonical Allele Identifier: CA470281526

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73122206G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362449G>C , CM000672.2:g.71362449G>C	GRCh38
NC_000010.10:g.73122206G>C , CM000672.1:g.73122206G>C	GRCh37
NC_000010.9:g.72792212G>C	NCBI36
NG_017066.1:g.48197G>C
NG_017066.2:g.48191G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2745G>C
ENST00000373189.6:c.1269G>C MANE Select	ENSP00000362285.5:p.Gly423=
ENST00000479577.2:c.1035G>C	ENSP00000493995.1:p.Gly345=
ENST00000642198.1:c.*841G>C	ENSP00000494827.1:n.*841G>C
ENST00000642772.1:c.*94+6206G>C	ENSP00000495041.1:n.*94+6206G>C
ENST00000643042.1:c.890G>C	ENSP00000496674.1:n.890G>C
ENST00000643619.1:c.*852G>C	ENSP00000494378.1:n.*852G>C
ENST00000643752.1:c.*595G>C	ENSP00000495000.1:n.*595G>C
ENST00000644088.1:c.*590G>C	ENSP00000494066.1:n.*590G>C
ENST00000644591.1:c.*595G>C	ENSP00000496664.1:n.*595G>C
ENST00000644895.1:c.*99+6206G>C	ENSP00000493872.1:n.*99+6206G>C
ENST00000645345.1:c.*841G>C	ENSP00000495859.1:n.*841G>C
ENST00000647524.1:c.*852G>C	ENSP00000495077.1:n.*852G>C
ENST00000373189.5:c.1269G>C	ENSP00000362285.5:p.Gly423=
ENST00000469204.1:n.766G>C
NM_001174098.1:c.*498G>C	NP_001167569.1:n.*498G>C
NM_018344.5:c.1269G>C	NP_060814.4:p.Gly423=
NR_033413.1:n.1243G>C
NR_033414.1:n.1016G>C
XM_006717910.2:c.1035G>C	XP_006717973.1:p.Gly345=
NM_001363518.1:c.1035G>C	NP_001350447.1:p.Gly345=
XM_017016377.2:c.831G>C	XP_016871866.1:p.Gly277=
XM_017016378.2:c.651G>C	XP_016871867.1:p.Gly217=
NM_018344.6:c.1269G>C MANE Select	NP_060814.4:p.Gly423=
NM_001174098.2:c.*498G>C	NP_001167569.1:n.*498G>C
NM_001363518.2:c.1035G>C	NP_001350447.1:p.Gly345=
NR_033413.2:n.1237G>C
NR_033414.2:n.1010G>C