Canonical Allele Identifier: CA2194345805

Gene: HAPLN3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.88881358C= , CM000677.2:g.88881358C=	GRCh38
NC_000015.9:g.89424589C= , CM000677.1:g.89424589C=	GRCh37
NC_000015.8:g.87225593C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359595.8:c.492G= MANE Select	ENSP00000352606.4:p.Arg164=
ENST00000359595.7:c.492G=	ENSP00000352606.3:p.Arg164=
ENST00000558770.5:c.492G=	ENSP00000456458.1:p.Arg164=
ENST00000562281.1:c.492G=	ENSP00000456985.1:p.Arg164=
ENST00000562889.5:c.678G=	ENSP00000457180.1:p.Arg226=
ENST00000563808.1:n.594G=
NM_001307952.1:c.678G=	NP_001294881.1:p.Arg226=
NM_178232.2:c.492G=	NP_839946.1:p.Arg164=
NM_178232.3:c.492G=	NP_839946.1:p.Arg164=
XM_011521261.1:c.624G=	XP_011519563.1:p.Arg208=
XR_243204.1:n.707G=
XR_931756.1:n.813G=
XM_017021934.2:c.678G=	XP_016877423.1:p.Arg226=
XM_017021935.2:c.113G=	XP_016877424.1:p.Gly38=
XM_017021936.2:c.113G=	XP_016877425.1:p.Gly38=
XR_001751098.2:n.825G=
XR_931756.3:n.826G=
NM_001307952.2:c.678G=	NP_001294881.1:p.Arg226=
NM_178232.4:c.492G= MANE Select	NP_839946.1:p.Arg164=