Canonical Allele Identifier: CA1363891691

Gene: HYAL2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50319551G= , CM000665.2:g.50319551G=	GRCh38
NC_000003.11:g.50356982G= , CM000665.1:g.50356982G=	GRCh37
NC_000003.10:g.50331986G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357750.9:c.921+18C= MANE Select	ENSP00000350387.4:n.921+18C=
ENST00000357750.8:c.921+18C=	ENSP00000350387.4:n.921+18C=
ENST00000395139.7:c.921+18C=	ENSP00000378571.3:n.921+18C=
ENST00000442581.1:c.921+18C=	ENSP00000406657.1:n.921+18C=
ENST00000447092.5:c.921+18C=	ENSP00000401853.1:n.921+18C=
ENST00000481597.5:n.1056+18C=
NM_003773.4:c.921+18C=	NP_003764.3:n.921+18C=
NM_033158.4:c.921+18C=	NP_149348.2:n.921+18C=
XM_005265524.1:c.921+18C=	XP_005265581.1:n.921+18C=
XM_005265525.1:c.921+18C=	XP_005265582.1:n.921+18C=
XM_005265524.2:c.921+18C=	XP_005265581.1:n.921+18C=
XM_005265525.2:c.921+18C=	XP_005265582.1:n.921+18C=
NM_003773.5:c.921+18C= MANE Select	NP_003764.3:n.921+18C=
NM_033158.5:c.921+18C=	NP_149348.2:n.921+18C=