Canonical Allele Identifier: CA2194345856

Gene: HAPLN3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.88881385T= , CM000677.2:g.88881385T=	GRCh38
NC_000015.9:g.89424616T= , CM000677.1:g.89424616T=	GRCh37
NC_000015.8:g.87225620T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359595.8:c.465A= MANE Select	ENSP00000352606.4:p.Glu155=
ENST00000359595.7:c.465A=	ENSP00000352606.3:p.Glu155=
ENST00000558770.5:c.465A=	ENSP00000456458.1:p.Glu155=
ENST00000562281.1:c.465A=	ENSP00000456985.1:p.Glu155=
ENST00000562889.5:c.651A=	ENSP00000457180.1:p.Glu217=
ENST00000563808.1:n.567A=
NM_001307952.1:c.651A=	NP_001294881.1:p.Glu217=
NM_178232.2:c.465A=	NP_839946.1:p.Glu155=
NM_178232.3:c.465A=	NP_839946.1:p.Glu155=
XM_011521261.1:c.597A=	XP_011519563.1:p.Glu199=
XR_243204.1:n.680A=
XR_931756.1:n.786A=
XM_017021934.2:c.651A=	XP_016877423.1:p.Glu217=
XM_017021935.2:c.86A=	XP_016877424.1:p.Lys29=
XM_017021936.2:c.86A=	XP_016877425.1:p.Lys29=
XR_001751098.2:n.798A=
XR_931756.3:n.799A=
NM_001307952.2:c.651A=	NP_001294881.1:p.Glu217=
NM_178232.4:c.465A= MANE Select	NP_839946.1:p.Glu155=