Canonical Allele Identifier: CA470281610

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73122260G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362503G>T , CM000672.2:g.71362503G>T	GRCh38
NC_000010.10:g.73122260G>T , CM000672.1:g.73122260G>T	GRCh37
NC_000010.9:g.72792266G>T	NCBI36
NG_017066.1:g.48251G>T
NG_017066.2:g.48245G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2799G>T
ENST00000373189.6:c.1323G>T MANE Select	ENSP00000362285.5:p.Val441=
ENST00000479577.2:c.1089G>T	ENSP00000493995.1:p.Val363=
ENST00000642198.1:c.*895G>T	ENSP00000494827.1:n.*895G>T
ENST00000642772.1:c.*94+6260G>T	ENSP00000495041.1:n.*94+6260G>T
ENST00000643042.1:c.944G>T	ENSP00000496674.1:n.944G>T
ENST00000643619.1:c.*906G>T	ENSP00000494378.1:n.*906G>T
ENST00000643752.1:c.*649G>T	ENSP00000495000.1:n.*649G>T
ENST00000644088.1:c.*644G>T	ENSP00000494066.1:n.*644G>T
ENST00000644591.1:c.*649G>T	ENSP00000496664.1:n.*649G>T
ENST00000644895.1:c.*99+6260G>T	ENSP00000493872.1:n.*99+6260G>T
ENST00000645345.1:c.*895G>T	ENSP00000495859.1:n.*895G>T
ENST00000647524.1:c.*906G>T	ENSP00000495077.1:n.*906G>T
ENST00000373189.5:c.1323G>T	ENSP00000362285.5:p.Val441=
ENST00000469204.1:n.820G>T
NM_001174098.1:c.*552G>T	NP_001167569.1:n.*552G>T
NM_018344.5:c.1323G>T	NP_060814.4:p.Val441=
NR_033413.1:n.1297G>T
NR_033414.1:n.1070G>T
XM_006717910.2:c.1089G>T	XP_006717973.1:p.Val363=
NM_001363518.1:c.1089G>T	NP_001350447.1:p.Val363=
XM_017016377.2:c.885G>T	XP_016871866.1:p.Val295=
XM_017016378.2:c.705G>T	XP_016871867.1:p.Val235=
NM_018344.6:c.1323G>T MANE Select	NP_060814.4:p.Val441=
NM_001174098.2:c.*552G>T	NP_001167569.1:n.*552G>T
NM_001363518.2:c.1089G>T	NP_001350447.1:p.Val363=
NR_033413.2:n.1291G>T
NR_033414.2:n.1064G>T