Canonical Allele Identifier: CA1363891834
Gene: HYAL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50319746G= , CM000665.2:g.50319746G= GRCh38
NC_000003.11:g.50357177G= , CM000665.1:g.50357177G= GRCh37
NC_000003.10:g.50332181G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000357750.9:c.744C= MANE Select ENSP00000350387.4:p.Leu248=
ENST00000357750.8:c.744C= ENSP00000350387.4:p.Leu248=
ENST00000395139.7:c.744C= ENSP00000378571.3:p.Leu248=
ENST00000442581.1:c.744C= ENSP00000406657.1:p.Leu248=
ENST00000447092.5:c.744C= ENSP00000401853.1:p.Leu248=
ENST00000481597.5:n.879C=
NM_003773.4:c.744C= NP_003764.3:p.Leu248=
NM_033158.4:c.744C= NP_149348.2:p.Leu248=
XM_005265524.1:c.744C= XP_005265581.1:p.Leu248=
XM_005265525.1:c.744C= XP_005265582.1:p.Leu248=
XM_005265524.2:c.744C= XP_005265581.1:p.Leu248=
XM_005265525.2:c.744C= XP_005265582.1:p.Leu248=
NM_003773.5:c.744C= MANE Select NP_003764.3:p.Leu248=
NM_033158.5:c.744C= NP_149348.2:p.Leu248=