Canonical Allele Identifier: CA2194346778

Gene: HAPLN3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.88881754A= , CM000677.2:g.88881754A=	GRCh38
NC_000015.9:g.89424985A= , CM000677.1:g.89424985A=	GRCh37
NC_000015.8:g.87225989A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359595.8:c.125-29T= MANE Select	ENSP00000352606.4:n.125-29T=
ENST00000359595.7:c.125-29T=	ENSP00000352606.3:n.125-29T=
ENST00000558770.5:c.125-29T=	ENSP00000456458.1:n.125-29T=
ENST00000562281.1:c.125-29T=	ENSP00000456985.1:n.125-29T=
ENST00000562889.5:c.311-29T=	ENSP00000457180.1:n.311-29T=
ENST00000563808.1:n.227-29T=
NM_001307952.1:c.311-29T=	NP_001294881.1:n.311-29T=
NM_178232.2:c.125-29T=	NP_839946.1:n.125-29T=
NM_178232.3:c.125-29T=	NP_839946.1:n.125-29T=
XM_011521261.1:c.257-29T=	XP_011519563.1:n.257-29T=
XR_243204.1:n.340-29T=
XR_931756.1:n.446-29T=
XM_017021934.2:c.311-29T=	XP_016877423.1:n.311-29T=
XM_017021935.2:c.-255-29T=	XP_016877424.1:n.-255-29T=
XM_017021936.2:c.-255-29T=	XP_016877425.1:n.-255-29T=
XR_001751098.2:n.458-29T=
XR_931756.3:n.459-29T=
NM_001307952.2:c.311-29T=	NP_001294881.1:n.311-29T=
NM_178232.4:c.125-29T= MANE Select	NP_839946.1:n.125-29T=