Canonical Allele Identifier: CA2796414560

Gene: SLC35E3

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.68746355_68746358del , CM000674.2:g.68746355_68746358del	GRCh38
NC_000012.11:g.69140135_69140138del , CM000674.1:g.69140135_69140138del	GRCh37
NC_000012.10:g.67426402_67426405del	NCBI36
NG_046600.2:g.64405_64408del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319429.7:n.221_224del
ENST00000398004.4:c.-23_-20del MANE Select	ENSP00000381089.2:n.-23_-20del
ENST00000673712.1:c.-23_-20del	ENSP00000501065.1:n.-23_-20del
ENST00000674096.1:c.-23_-20del	ENSP00000501130.1:n.-23_-20del
ENST00000398004.3:c.-23_-20del	ENSP00000381089.2:n.-23_-20del
NM_018656.2:c.-23_-20del	NP_061126.2:n.-23_-20del
XM_005269006.2:c.-23_-20del	XP_005269063.1:n.-23_-20del
NM_001354997.1:c.-23_-20del	NP_001341926.1:n.-23_-20del
NM_001354998.1:c.-23_-20del	NP_001341927.1:n.-23_-20del
NM_018656.3:c.-23_-20del	NP_061126.2:n.-23_-20del
NR_149143.1:n.270_273del
NR_149144.1:n.270_273del
NM_001354997.3:c.-23_-20del	NP_001341926.1:n.-23_-20del
NM_001354998.2:c.-23_-20del	NP_001341927.1:n.-23_-20del
NM_018656.5:c.-23_-20del MANE Select	NP_061126.2:n.-23_-20del
NR_149143.3:n.180_183del
NR_149144.3:n.180_183del