Canonical Allele Identifier: CA1363888527

Gene: HYAL1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50302155C= , CM000665.2:g.50302155C=	GRCh38
NC_000003.11:g.50339586C= , CM000665.1:g.50339586C=	GRCh37
NC_000003.10:g.50314590C=	NCBI36
NG_009295.1:g.15227G=

Transcript Alleles

HGVS	Amino-acid Change
NM_033159.4:c.802G= MANE Select	NP_149349.2:p.Glu268=
ENST00000395144.7:c.802G= MANE Select	ENSP00000378576.2:p.Glu268=
NM_033159.3:c.802G=	NP_149349.2:p.Glu268=
NM_153281.1:c.802G=	NP_695013.1:p.Glu268=
NM_153281.2:c.802G=	NP_695013.1:p.Glu268=
NM_153282.2:c.802G=	NP_695014.1:p.Glu268=
NM_153282.3:c.802G=	NP_695014.1:p.Glu268=
NM_153283.2:c.256G=	NP_695015.1:p.Glu86=
NM_153283.3:c.256G=	NP_695015.1:p.Glu86=
NM_153285.2:c.25G=	NP_695017.1:p.Glu9=
NM_153285.3:c.25G=	NP_695017.1:p.Glu9=
NR_047690.1:n.1447G=
NR_047690.2:n.1420G=
ENST00000266031.8:c.802G=	ENSP00000266031.4:p.Glu268=
ENST00000320295.12:c.802G=	ENSP00000346068.5:p.Glu268=
ENST00000395143.6:c.802G=	ENSP00000378575.2:p.Glu268=
ENST00000395144.6:c.802G=	ENSP00000378576.2:p.Glu268=
ENST00000447605.2:c.25G=	ENSP00000390149.2:p.Glu9=
ENST00000457214.6:c.256G=	ENSP00000393358.2:p.Glu86=
ENST00000618175.4:c.802G=	ENSP00000477903.1:p.Glu268=
XM_011533667.1:c.802G=	XP_011531969.1:p.Glu268=
XM_011533667.2:c.802G=	XP_011531969.1:p.Glu268=
XM_011533668.1:c.802G=	XP_011531970.1:p.Glu268=
XM_011533668.2:c.802G=	XP_011531970.1:p.Glu268=
XM_011533669.1:c.802G=	XP_011531971.1:p.Glu268=
XM_011533669.2:c.802G=	XP_011531971.1:p.Glu268=