Canonical Allele Identifier: CA470280899

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73121795G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362038G>T , CM000672.2:g.71362038G>T	GRCh38
NC_000010.10:g.73121795G>T , CM000672.1:g.73121795G>T	GRCh37
NC_000010.9:g.72791801G>T	NCBI36
NG_017066.1:g.47786G>T
NG_017066.2:g.47780G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2334G>T
ENST00000373189.6:c.858G>T MANE Select	ENSP00000362285.5:p.Val286=
ENST00000479577.2:c.624G>T	ENSP00000493995.1:p.Val208=
ENST00000642198.1:c.*430G>T	ENSP00000494827.1:n.*430G>T
ENST00000642772.1:c.*94+5795G>T	ENSP00000495041.1:n.*94+5795G>T
ENST00000643042.1:c.479G>T	ENSP00000496674.1:n.479G>T
ENST00000643619.1:c.*441G>T	ENSP00000494378.1:n.*441G>T
ENST00000643752.1:c.*184G>T	ENSP00000495000.1:n.*184G>T
ENST00000644088.1:c.*179G>T	ENSP00000494066.1:n.*179G>T
ENST00000644591.1:c.*184G>T	ENSP00000496664.1:n.*184G>T
ENST00000644895.1:c.*99+5795G>T	ENSP00000493872.1:n.*99+5795G>T
ENST00000645345.1:c.*430G>T	ENSP00000495859.1:n.*430G>T
ENST00000647524.1:c.*441G>T	ENSP00000495077.1:n.*441G>T
ENST00000373189.5:c.858G>T	ENSP00000362285.5:p.Val286=
ENST00000469204.1:n.355G>T
NM_001174098.1:c.*87G>T	NP_001167569.1:n.*87G>T
NM_018344.5:c.858G>T	NP_060814.4:p.Val286=
NR_033413.1:n.832G>T
NR_033414.1:n.605G>T
XM_006717910.2:c.624G>T	XP_006717973.1:p.Val208=
NM_001363518.1:c.624G>T	NP_001350447.1:p.Val208=
XM_017016377.2:c.420G>T	XP_016871866.1:p.Val140=
XM_017016378.2:c.240G>T	XP_016871867.1:p.Val80=
NM_018344.6:c.858G>T MANE Select	NP_060814.4:p.Val286=
NM_001174098.2:c.*87G>T	NP_001167569.1:n.*87G>T
NM_001363518.2:c.624G>T	NP_001350447.1:p.Val208=
NR_033413.2:n.826G>T
NR_033414.2:n.599G>T