Canonical Allele Identifier: CA470281162

Gene: SLC29A3

Linked Data

• gnomAD v4: 10-71362143-C-T
• MyVariant Identifiers: chr10:g.73121900C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362143C>T , CM000672.2:g.71362143C>T	GRCh38
NC_000010.10:g.73121900C>T , CM000672.1:g.73121900C>T	GRCh37
NC_000010.9:g.72791906C>T	NCBI36
NG_017066.1:g.47891C>T
NG_017066.2:g.47885C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2439C>T
ENST00000373189.6:c.963C>T MANE Select	ENSP00000362285.5:p.Leu321=
ENST00000479577.2:c.729C>T	ENSP00000493995.1:p.Leu243=
ENST00000642198.1:c.*535C>T	ENSP00000494827.1:n.*535C>T
ENST00000642772.1:c.*94+5900C>T	ENSP00000495041.1:n.*94+5900C>T
ENST00000643042.1:c.584C>T	ENSP00000496674.1:n.584C>T
ENST00000643619.1:c.*546C>T	ENSP00000494378.1:n.*546C>T
ENST00000643752.1:c.*289C>T	ENSP00000495000.1:n.*289C>T
ENST00000644088.1:c.*284C>T	ENSP00000494066.1:n.*284C>T
ENST00000644591.1:c.*289C>T	ENSP00000496664.1:n.*289C>T
ENST00000644895.1:c.*99+5900C>T	ENSP00000493872.1:n.*99+5900C>T
ENST00000645345.1:c.*535C>T	ENSP00000495859.1:n.*535C>T
ENST00000647524.1:c.*546C>T	ENSP00000495077.1:n.*546C>T
ENST00000373189.5:c.963C>T	ENSP00000362285.5:p.Leu321=
ENST00000469204.1:n.460C>T
NM_001174098.1:c.*192C>T	NP_001167569.1:n.*192C>T
NM_018344.5:c.963C>T	NP_060814.4:p.Leu321=
NR_033413.1:n.937C>T
NR_033414.1:n.710C>T
XM_006717910.2:c.729C>T	XP_006717973.1:p.Leu243=
NM_001363518.1:c.729C>T	NP_001350447.1:p.Leu243=
XM_017016377.2:c.525C>T	XP_016871866.1:p.Leu175=
XM_017016378.2:c.345C>T	XP_016871867.1:p.Leu115=
NM_018344.6:c.963C>T MANE Select	NP_060814.4:p.Leu321=
NM_001174098.2:c.*192C>T	NP_001167569.1:n.*192C>T
NM_001363518.2:c.729C>T	NP_001350447.1:p.Leu243=
NR_033413.2:n.931C>T
NR_033414.2:n.704C>T