Canonical Allele Identifier: CA1363891848

Gene: HYAL2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50319752C= , CM000665.2:g.50319752C=	GRCh38
NC_000003.11:g.50357183C= , CM000665.1:g.50357183C=	GRCh37
NC_000003.10:g.50332187C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000357750.9:c.738G= MANE Select	ENSP00000350387.4:p.Thr246=
ENST00000357750.8:c.738G=	ENSP00000350387.4:p.Thr246=
ENST00000395139.7:c.738G=	ENSP00000378571.3:p.Thr246=
ENST00000442581.1:c.738G=	ENSP00000406657.1:p.Thr246=
ENST00000447092.5:c.738G=	ENSP00000401853.1:p.Thr246=
ENST00000481597.5:n.873G=
NM_003773.4:c.738G=	NP_003764.3:p.Thr246=
NM_033158.4:c.738G=	NP_149348.2:p.Thr246=
XM_005265524.1:c.738G=	XP_005265581.1:p.Thr246=
XM_005265525.1:c.738G=	XP_005265582.1:p.Thr246=
XM_005265524.2:c.738G=	XP_005265581.1:p.Thr246=
XM_005265525.2:c.738G=	XP_005265582.1:p.Thr246=
NM_003773.5:c.738G= MANE Select	NP_003764.3:p.Thr246=
NM_033158.5:c.738G=	NP_149348.2:p.Thr246=