Canonical Allele Identifier: CA2194345859

Gene: HAPLN3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.88881392T= , CM000677.2:g.88881392T=	GRCh38
NC_000015.9:g.89424623T= , CM000677.1:g.89424623T=	GRCh37
NC_000015.8:g.87225627T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359595.8:c.458A= MANE Select	ENSP00000352606.4:p.Glu153=
ENST00000359595.7:c.458A=	ENSP00000352606.3:p.Glu153=
ENST00000558770.5:c.458A=	ENSP00000456458.1:p.Glu153=
ENST00000562281.1:c.458A=	ENSP00000456985.1:p.Glu153=
ENST00000562889.5:c.644A=	ENSP00000457180.1:p.Glu215=
ENST00000563808.1:n.560A=
NM_001307952.1:c.644A=	NP_001294881.1:p.Glu215=
NM_178232.2:c.458A=	NP_839946.1:p.Glu153=
NM_178232.3:c.458A=	NP_839946.1:p.Glu153=
XM_011521261.1:c.590A=	XP_011519563.1:p.Glu197=
XR_243204.1:n.673A=
XR_931756.1:n.779A=
XM_017021934.2:c.644A=	XP_016877423.1:p.Glu215=
XM_017021935.2:c.79A=	XP_016877424.1:p.Arg27=
XM_017021936.2:c.79A=	XP_016877425.1:p.Arg27=
XR_001751098.2:n.791A=
XR_931756.3:n.792A=
NM_001307952.2:c.644A=	NP_001294881.1:p.Glu215=
NM_178232.4:c.458A= MANE Select	NP_839946.1:p.Glu153=