Canonical Allele Identifier: CA377116131

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73122003A>G (hg19) ; chr10:g.71362246A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362246A>G , CM000672.2:g.71362246A>G	GRCh38
NC_000010.10:g.73122003A>G , CM000672.1:g.73122003A>G	GRCh37
NC_000010.9:g.72792009A>G	NCBI36
NG_017066.1:g.47994A>G
NG_017066.2:g.47988A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2542A>G
ENST00000373189.6:c.1066A>G MANE Select	ENSP00000362285.5:p.Asn356Asp
ENST00000479577.2:c.832A>G	ENSP00000493995.1:p.Asn278Asp
ENST00000642198.1:c.*638A>G	ENSP00000494827.1:n.*638A>G
ENST00000642772.1:c.*94+6003A>G	ENSP00000495041.1:n.*94+6003A>G
ENST00000643042.1:c.687A>G	ENSP00000496674.1:n.687A>G
ENST00000643619.1:c.*649A>G	ENSP00000494378.1:n.*649A>G
ENST00000643752.1:c.*392A>G	ENSP00000495000.1:n.*392A>G
ENST00000644088.1:c.*387A>G	ENSP00000494066.1:n.*387A>G
ENST00000644591.1:c.*392A>G	ENSP00000496664.1:n.*392A>G
ENST00000644895.1:c.*99+6003A>G	ENSP00000493872.1:n.*99+6003A>G
ENST00000645345.1:c.*638A>G	ENSP00000495859.1:n.*638A>G
ENST00000647524.1:c.*649A>G	ENSP00000495077.1:n.*649A>G
ENST00000373189.5:c.1066A>G	ENSP00000362285.5:p.Asn356Asp
ENST00000469204.1:n.563A>G
NM_001174098.1:c.*295A>G	NP_001167569.1:n.*295A>G
NM_018344.5:c.1066A>G	NP_060814.4:p.Asn356Asp
NR_033413.1:n.1040A>G
NR_033414.1:n.813A>G
XM_006717910.2:c.832A>G	XP_006717973.1:p.Asn278Asp
NM_001363518.1:c.832A>G	NP_001350447.1:p.Asn278Asp
XM_017016377.2:c.628A>G	XP_016871866.1:p.Asn210Asp
XM_017016378.2:c.448A>G	XP_016871867.1:p.Asn150Asp
NM_018344.6:c.1066A>G MANE Select	NP_060814.4:p.Asn356Asp
NM_001174098.2:c.*295A>G	NP_001167569.1:n.*295A>G
NM_001363518.2:c.832A>G	NP_001350447.1:p.Asn278Asp
NR_033413.2:n.1034A>G
NR_033414.2:n.807A>G