Canonical Allele Identifier: CA377128556

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71319312T>G , CM000672.2:g.71319312T>G	GRCh38
NC_000010.10:g.73079069T>G , CM000672.1:g.73079069T>G	GRCh37
NC_000010.9:g.72749075T>G	NCBI36
NG_017066.1:g.5060T>G
NG_017066.2:g.5054T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_018344.6:c.1+2T>G MANE Select	NP_060814.4:n.1+2T>G
ENST00000373189.6:c.1+2T>G MANE Select	ENSP00000362285.5:n.1+2T>G
NM_001174098.1:c.1+2T>G	NP_001167569.1:n.1+2T>G
NM_001174098.2:c.1+2T>G	NP_001167569.1:n.1+2T>G
NM_001363518.1:c.-653T>G	NP_001350447.1:n.-653T>G
NM_001363518.2:c.-653T>G	NP_001350447.1:n.-653T>G
NM_018344.5:c.1+2T>G	NP_060814.4:n.1+2T>G
NR_033413.1:n.58+2T>G
NR_033413.2:n.52+2T>G
NR_033414.1:n.58+2T>G
NR_033414.2:n.52+2T>G
ENST00000373189.5:c.1+2T>G	ENSP00000362285.5:n.1+2T>G
ENST00000479577.1:n.31T>G
ENST00000479577.2:c.-653T>G	ENSP00000493995.1:n.-653T>G
ENST00000642772.1:c.1+2T>G	ENSP00000495041.1:n.1+2T>G
ENST00000643752.1:c.1+2T>G	ENSP00000495000.1:n.1+2T>G
ENST00000644088.1:c.1+2T>G	ENSP00000494066.1:n.1+2T>G
ENST00000644591.1:c.1+2T>G	ENSP00000496664.1:n.1+2T>G
ENST00000644895.1:c.1+2T>G	ENSP00000493872.1:n.1+2T>G
ENST00000645345.1:c.1+2T>G	ENSP00000495859.1:n.1+2T>G
ENST00000647524.1:c.1+2T>G	ENSP00000495077.1:n.1+2T>G
ENST00000697843.1:n.28T>G
XM_006717910.2:c.-653T>G	XP_006717973.1:n.-653T>G
XM_017016377.2:c.-774T>G	XP_016871866.1:n.-774T>G
XM_017016378.2:c.-727T>G	XP_016871867.1:n.-727T>G