Canonical Allele Identifier: CA1918670595

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71344317_71344323delinsGGCCTCT , CM000672.2:g.71344317_71344323delinsGGCCTCT	GRCh38
NC_000010.10:g.73104074_73104080delinsGGCCTCT , CM000672.1:g.73104074_73104080delinsGGCCTCT	GRCh37
NC_000010.9:g.72774080_72774086delinsGGCCTCT	NCBI36
NG_017066.1:g.30065_30071delinsGGCCTCT
NG_017066.2:g.30059_30065delinsGGCCTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.829+26_829+32delinsGGCCTCT
ENST00000373189.6:c.383+26_383+32delinsGGCCTCT MANE Select	ENSP00000362285.5:n.383+26_383+32delinsGGCCTCT
ENST00000479577.2:c.149+26_149+32delinsGGCCTCT	ENSP00000493995.1:n.149+26_149+32delinsGGCCTCT
ENST00000642198.1:c.67-7245_67-7239delinsGGCCTCT	ENSP00000494827.1:n.67-7245_67-7239delinsGGCCTCT
ENST00000642772.1:c.301-11764_301-11758delinsGGCCTCT	ENSP00000495041.1:n.301-11764_301-11758delinsGGCCTCT
ENST00000643042.1:c.232-11764_232-11758delinsGGCCTCT	ENSP00000496674.1:n.232-11764_232-11758delinsGGCCTCT
ENST00000643619.1:c.149+26_149+32delinsGGCCTCT	ENSP00000494378.1:n.149+26_149+32delinsGGCCTCT
ENST00000643752.1:c.383+26_383+32delinsGGCCTCT	ENSP00000495000.1:n.383+26_383+32delinsGGCCTCT
ENST00000644088.1:c.301-11764_301-11758delinsGGCCTCT	ENSP00000494066.1:n.301-11764_301-11758delinsGGCCTCT
ENST00000644591.1:c.301-7245_301-7239delinsGGCCTCT	ENSP00000496664.1:n.301-7245_301-7239delinsGGCCTCT
ENST00000644895.1:c.301-7245_301-7239delinsGGCCTCT	ENSP00000493872.1:n.301-7245_301-7239delinsGGCCTCT
ENST00000645345.1:c.301-7245_301-7239delinsGGCCTCT	ENSP00000495859.1:n.301-7245_301-7239delinsGGCCTCT
ENST00000647524.1:c.383+26_383+32delinsGGCCTCT	ENSP00000495077.1:n.383+26_383+32delinsGGCCTCT
ENST00000373189.5:c.383+26_383+32delinsGGCCTCT	ENSP00000362285.5:n.383+26_383+32delinsGGCCTCT
NM_001174098.1:c.383+26_383+32delinsGGCCTCT	NP_001167569.1:n.383+26_383+32delinsGGCCTCT
NM_018344.5:c.383+26_383+32delinsGGCCTCT	NP_060814.4:n.383+26_383+32delinsGGCCTCT
NR_033413.1:n.358-7245_358-7239delinsGGCCTCT
NR_033414.1:n.358-11764_358-11758delinsGGCCTCT
XM_006717910.2:c.149+26_149+32delinsGGCCTCT	XP_006717973.1:n.149+26_149+32delinsGGCCTCT
XR_946051.1:n.626-2942_626-2936delinsAGAGGCC
NM_001363518.1:c.149+26_149+32delinsGGCCTCT	NP_001350447.1:n.149+26_149+32delinsGGCCTCT
XM_017016377.2:c.-55-7245_-55-7239delinsGGCCTCT	XP_016871866.1:n.-55-7245_-55-7239delinsGGCCTCT
XM_017016378.2:c.-8-11764_-8-11758delinsGGCCTCT	XP_016871867.1:n.-8-11764_-8-11758delinsGGCCTCT
XR_001747496.1:n.1552-2942_1552-2936delinsAGAGGCC
XR_946051.2:n.1552-2942_1552-2936delinsAGAGGCC
NM_018344.6:c.383+26_383+32delinsGGCCTCT MANE Select	NP_060814.4:n.383+26_383+32delinsGGCCTCT
NM_001174098.2:c.383+26_383+32delinsGGCCTCT	NP_001167569.1:n.383+26_383+32delinsGGCCTCT
NM_001363518.2:c.149+26_149+32delinsGGCCTCT	NP_001350447.1:n.149+26_149+32delinsGGCCTCT
NR_033413.2:n.352-7245_352-7239delinsGGCCTCT
NR_033414.2:n.352-11764_352-11758delinsGGCCTCT