Canonical Allele Identifier: CA2521243826

Gene: SLC35A2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48905495_48905496del , CM000685.2:g.48905495_48905496del	GRCh38
NC_000023.10:g.48762772_48762773del , CM000685.1:g.48762772_48762773del	GRCh37
NC_000023.9:g.48647716_48647717del	NCBI36
NG_034300.1:g.11463_11464del

Transcript Alleles

HGVS	Amino-acid change
ENST00000247138.11:c.427-14_427-13del MANE Select	ENSP00000247138.5:n.427-14_427-13del
ENST00000247138.10:c.427-14_427-13del	ENSP00000247138.5:n.427-14_427-13del
ENST00000376515.8:c.355-604_355-603del	ENSP00000365698.3:n.355-604_355-603del
ENST00000376521.6:c.427-14_427-13del	ENSP00000365704.1:n.427-14_427-13del
ENST00000376529.8:c.427-604_427-603del	ENSP00000365712.3:n.427-604_427-603del
ENST00000413561.7:c.212-237_212-236del
ENST00000445167.7:c.427-604_427-603del	ENSP00000402726.2:n.427-604_427-603del
ENST00000446885.1:c.211-14_211-13del	ENSP00000415518.1:n.211-14_211-13del
ENST00000452555.7:c.511-14_511-13del	ENSP00000416002.2:n.511-14_511-13del
ENST00000616181.5:c.466-14_466-13del	ENSP00000478617.1:n.466-14_466-13del
ENST00000634665.1:c.*47-14_*47-13del	ENSP00000489356.1:n.*47-14_*47-13del
ENST00000635238.1:c.388-14_388-13del	ENSP00000489515.1:n.388-14_388-13del
ENST00000635285.1:c.427-14_427-13del	ENSP00000489484.1:n.427-14_427-13del
ENST00000635460.1:c.424+896_424+897del
ENST00000635589.1:c.244-14_244-13del	ENSP00000489197.1:n.244-14_244-13del
ENST00000635628.1:c.*321-14_*321-13del	ENSP00000489613.1:n.*321-14_*321-13del
NM_001032289.2:c.427-604_427-603del	NP_001027460.1:n.427-604_427-603del
NM_001042498.2:c.427-14_427-13del	NP_001035963.1:n.427-14_427-13del
NM_001282647.1:c.427-604_427-603del	NP_001269576.1:n.427-604_427-603del
NM_001282648.1:c.355-604_355-603del	NP_001269577.1:n.355-604_355-603del
NM_001282649.1:c.244-14_244-13del	NP_001269578.1:n.244-14_244-13del
NM_001282650.1:c.466-14_466-13del	NP_001269579.1:n.466-14_466-13del
NM_001282651.1:c.511-14_511-13del	NP_001269580.1:n.511-14_511-13del
NM_005660.2:c.427-14_427-13del	NP_005651.1:n.427-14_427-13del
NM_005660.3:c.427-14_427-13del MANE Select	NP_005651.1:n.427-14_427-13del
NM_001032289.3:c.427-604_427-603del	NP_001027460.1:n.427-604_427-603del
NM_001042498.3:c.427-14_427-13del	NP_001035963.1:n.427-14_427-13del
NM_001282647.2:c.427-604_427-603del	NP_001269576.1:n.427-604_427-603del
NM_001282649.2:c.244-14_244-13del	NP_001269578.1:n.244-14_244-13del
NM_001282650.2:c.466-14_466-13del	NP_001269579.1:n.466-14_466-13del
NM_001282651.2:c.511-14_511-13del	NP_001269580.1:n.511-14_511-13del
NM_001282648.2:c.355-604_355-603del	NP_001269577.1:n.355-604_355-603del