Canonical Allele Identifier: CA2756211162
Gene: HYAL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50319537_50319555del , CM000665.2:g.50319537_50319555del GRCh38
NC_000003.11:g.50356968_50356986del , CM000665.1:g.50356968_50356986del GRCh37
NC_000003.10:g.50331972_50331990del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000357750.9:c.921+14_921+32del MANE Select ENSP00000350387.4:n.921+14_921+32del
ENST00000357750.8:c.921+14_921+32del ENSP00000350387.4:n.921+14_921+32del
ENST00000395139.7:c.921+14_921+32del ENSP00000378571.3:n.921+14_921+32del
ENST00000442581.1:c.921+14_921+32del ENSP00000406657.1:n.921+14_921+32del
ENST00000447092.5:c.921+14_921+32del ENSP00000401853.1:n.921+14_921+32del
ENST00000481597.5:n.1056+14_1056+32del
NM_003773.4:c.921+14_921+32del NP_003764.3:n.921+14_921+32del
NM_033158.4:c.921+14_921+32del NP_149348.2:n.921+14_921+32del
XM_005265524.1:c.921+14_921+32del XP_005265581.1:n.921+14_921+32del
XM_005265525.1:c.921+14_921+32del XP_005265582.1:n.921+14_921+32del
XM_005265524.2:c.921+14_921+32del XP_005265581.1:n.921+14_921+32del
XM_005265525.2:c.921+14_921+32del XP_005265582.1:n.921+14_921+32del
NM_003773.5:c.921+14_921+32del MANE Select NP_003764.3:n.921+14_921+32del
NM_033158.5:c.921+14_921+32del NP_149348.2:n.921+14_921+32del