Canonical Allele Identifier: CA2194346339

Gene: HAPLN3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.88881588A= , CM000677.2:g.88881588A=	GRCh38
NC_000015.9:g.89424819A= , CM000677.1:g.89424819A=	GRCh37
NC_000015.8:g.87225823A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359595.8:c.262T= MANE Select	ENSP00000352606.4:p.Trp88=
ENST00000359595.7:c.262T=	ENSP00000352606.3:p.Trp88=
ENST00000558770.5:c.262T=	ENSP00000456458.1:p.Trp88=
ENST00000562281.1:c.262T=	ENSP00000456985.1:p.Trp88=
ENST00000562889.5:c.448T=	ENSP00000457180.1:p.Trp150=
ENST00000563808.1:n.364T=
NM_001307952.1:c.448T=	NP_001294881.1:p.Trp150=
NM_178232.2:c.262T=	NP_839946.1:p.Trp88=
NM_178232.3:c.262T=	NP_839946.1:p.Trp88=
XM_011521261.1:c.394T=	XP_011519563.1:p.Trp132=
XR_243204.1:n.477T=
XR_931756.1:n.583T=
XM_017021934.2:c.448T=	XP_016877423.1:p.Trp150=
XM_017021935.2:c.-118T=	XP_016877424.1:n.-118T=
XM_017021936.2:c.-118T=	XP_016877425.1:n.-118T=
XR_001751098.2:n.595T=
XR_931756.3:n.596T=
NM_001307952.2:c.448T=	NP_001294881.1:p.Trp150=
NM_178232.4:c.262T= MANE Select	NP_839946.1:p.Trp88=