Canonical Allele Identifier: CA2194345965

Gene: HAPLN3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.88881417G= , CM000677.2:g.88881417G=	GRCh38
NC_000015.9:g.89424648G= , CM000677.1:g.89424648G=	GRCh37
NC_000015.8:g.87225652G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359595.8:c.433C= MANE Select	ENSP00000352606.4:p.Arg145=
ENST00000359595.7:c.433C=	ENSP00000352606.3:p.Arg145=
ENST00000558770.5:c.433C=	ENSP00000456458.1:p.Arg145=
ENST00000562281.1:c.433C=	ENSP00000456985.1:p.Arg145=
ENST00000562889.5:c.619C=	ENSP00000457180.1:p.Arg207=
ENST00000563808.1:n.535C=
NM_001307952.1:c.619C=	NP_001294881.1:p.Arg207=
NM_178232.2:c.433C=	NP_839946.1:p.Arg145=
NM_178232.3:c.433C=	NP_839946.1:p.Arg145=
XM_011521261.1:c.565C=	XP_011519563.1:p.Arg189=
XR_243204.1:n.648C=
XR_931756.1:n.754C=
XM_017021934.2:c.619C=	XP_016877423.1:p.Arg207=
XM_017021935.2:c.54C=	XP_016877424.1:p.Thr18=
XM_017021936.2:c.54C=	XP_016877425.1:p.Thr18=
XR_001751098.2:n.766C=
XR_931756.3:n.767C=
NM_001307952.2:c.619C=	NP_001294881.1:p.Arg207=
NM_178232.4:c.433C= MANE Select	NP_839946.1:p.Arg145=