Canonical Allele Identifier: CA377117233

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73122246G>T (hg19) ; chr10:g.71362489G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362489G>T , CM000672.2:g.71362489G>T	GRCh38
NC_000010.10:g.73122246G>T , CM000672.1:g.73122246G>T	GRCh37
NC_000010.9:g.72792252G>T	NCBI36
NG_017066.1:g.48237G>T
NG_017066.2:g.48231G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2785G>T
ENST00000373189.6:c.1309G>T MANE Select	ENSP00000362285.5:p.Gly437Trp
ENST00000479577.2:c.1075G>T	ENSP00000493995.1:p.Gly359Trp
ENST00000642198.1:c.*881G>T	ENSP00000494827.1:n.*881G>T
ENST00000642772.1:c.*94+6246G>T	ENSP00000495041.1:n.*94+6246G>T
ENST00000643042.1:c.930G>T	ENSP00000496674.1:n.930G>T
ENST00000643619.1:c.*892G>T	ENSP00000494378.1:n.*892G>T
ENST00000643752.1:c.*635G>T	ENSP00000495000.1:n.*635G>T
ENST00000644088.1:c.*630G>T	ENSP00000494066.1:n.*630G>T
ENST00000644591.1:c.*635G>T	ENSP00000496664.1:n.*635G>T
ENST00000644895.1:c.*99+6246G>T	ENSP00000493872.1:n.*99+6246G>T
ENST00000645345.1:c.*881G>T	ENSP00000495859.1:n.*881G>T
ENST00000647524.1:c.*892G>T	ENSP00000495077.1:n.*892G>T
ENST00000373189.5:c.1309G>T	ENSP00000362285.5:p.Gly437Trp
ENST00000469204.1:n.806G>T
NM_001174098.1:c.*538G>T	NP_001167569.1:n.*538G>T
NM_018344.5:c.1309G>T	NP_060814.4:p.Gly437Trp
NR_033413.1:n.1283G>T
NR_033414.1:n.1056G>T
XM_006717910.2:c.1075G>T	XP_006717973.1:p.Gly359Trp
NM_001363518.1:c.1075G>T	NP_001350447.1:p.Gly359Trp
XM_017016377.2:c.871G>T	XP_016871866.1:p.Gly291Trp
XM_017016378.2:c.691G>T	XP_016871867.1:p.Gly231Trp
NM_018344.6:c.1309G>T MANE Select	NP_060814.4:p.Gly437Trp
NM_001174098.2:c.*538G>T	NP_001167569.1:n.*538G>T
NM_001363518.2:c.1075G>T	NP_001350447.1:p.Gly359Trp
NR_033413.2:n.1277G>T
NR_033414.2:n.1050G>T