Canonical Allele Identifier: CA377114913

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73121867C>A (hg19) ; chr10:g.71362110C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362110C>A , CM000672.2:g.71362110C>A	GRCh38
NC_000010.10:g.73121867C>A , CM000672.1:g.73121867C>A	GRCh37
NC_000010.9:g.72791873C>A	NCBI36
NG_017066.1:g.47858C>A
NG_017066.2:g.47852C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2406C>A
ENST00000373189.6:c.930C>A MANE Select	ENSP00000362285.5:p.Phe310Leu
ENST00000479577.2:c.696C>A	ENSP00000493995.1:p.Phe232Leu
ENST00000642198.1:c.*502C>A	ENSP00000494827.1:n.*502C>A
ENST00000642772.1:c.*94+5867C>A	ENSP00000495041.1:n.*94+5867C>A
ENST00000643042.1:c.551C>A	ENSP00000496674.1:n.551C>A
ENST00000643619.1:c.*513C>A	ENSP00000494378.1:n.*513C>A
ENST00000643752.1:c.*256C>A	ENSP00000495000.1:n.*256C>A
ENST00000644088.1:c.*251C>A	ENSP00000494066.1:n.*251C>A
ENST00000644591.1:c.*256C>A	ENSP00000496664.1:n.*256C>A
ENST00000644895.1:c.*99+5867C>A	ENSP00000493872.1:n.*99+5867C>A
ENST00000645345.1:c.*502C>A	ENSP00000495859.1:n.*502C>A
ENST00000647524.1:c.*513C>A	ENSP00000495077.1:n.*513C>A
ENST00000373189.5:c.930C>A	ENSP00000362285.5:p.Phe310Leu
ENST00000469204.1:n.427C>A
NM_001174098.1:c.*159C>A	NP_001167569.1:n.*159C>A
NM_018344.5:c.930C>A	NP_060814.4:p.Phe310Leu
NR_033413.1:n.904C>A
NR_033414.1:n.677C>A
XM_006717910.2:c.696C>A	XP_006717973.1:p.Phe232Leu
NM_001363518.1:c.696C>A	NP_001350447.1:p.Phe232Leu
XM_017016377.2:c.492C>A	XP_016871866.1:p.Phe164Leu
XM_017016378.2:c.312C>A	XP_016871867.1:p.Phe104Leu
NM_018344.6:c.930C>A MANE Select	NP_060814.4:p.Phe310Leu
NM_001174098.2:c.*159C>A	NP_001167569.1:n.*159C>A
NM_001363518.2:c.696C>A	NP_001350447.1:p.Phe232Leu
NR_033413.2:n.898C>A
NR_033414.2:n.671C>A