Canonical Allele Identifier: CA1363891694

Gene: HYAL2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50319553C= , CM000665.2:g.50319553C=	GRCh38
NC_000003.11:g.50356984C= , CM000665.1:g.50356984C=	GRCh37
NC_000003.10:g.50331988C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357750.9:c.921+16G= MANE Select	ENSP00000350387.4:n.921+16G=
ENST00000357750.8:c.921+16G=	ENSP00000350387.4:n.921+16G=
ENST00000395139.7:c.921+16G=	ENSP00000378571.3:n.921+16G=
ENST00000442581.1:c.921+16G=	ENSP00000406657.1:n.921+16G=
ENST00000447092.5:c.921+16G=	ENSP00000401853.1:n.921+16G=
ENST00000481597.5:n.1056+16G=
NM_003773.4:c.921+16G=	NP_003764.3:n.921+16G=
NM_033158.4:c.921+16G=	NP_149348.2:n.921+16G=
XM_005265524.1:c.921+16G=	XP_005265581.1:n.921+16G=
XM_005265525.1:c.921+16G=	XP_005265582.1:n.921+16G=
XM_005265524.2:c.921+16G=	XP_005265581.1:n.921+16G=
XM_005265525.2:c.921+16G=	XP_005265582.1:n.921+16G=
NM_003773.5:c.921+16G= MANE Select	NP_003764.3:n.921+16G=
NM_033158.5:c.921+16G=	NP_149348.2:n.921+16G=