Canonical Allele Identifier: CA2194346058

Gene: HAPLN3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.88881456C= , CM000677.2:g.88881456C=	GRCh38
NC_000015.9:g.89424687C= , CM000677.1:g.89424687C=	GRCh37
NC_000015.8:g.87225691C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000359595.8:c.394G= MANE Select	ENSP00000352606.4:p.Glu132=
ENST00000359595.7:c.394G=	ENSP00000352606.3:p.Glu132=
ENST00000558770.5:c.394G=	ENSP00000456458.1:p.Glu132=
ENST00000562281.1:c.394G=	ENSP00000456985.1:p.Glu132=
ENST00000562889.5:c.580G=	ENSP00000457180.1:p.Glu194=
ENST00000563808.1:n.496G=
NM_001307952.1:c.580G=	NP_001294881.1:p.Glu194=
NM_178232.2:c.394G=	NP_839946.1:p.Glu132=
NM_178232.3:c.394G=	NP_839946.1:p.Glu132=
XM_011521261.1:c.526G=	XP_011519563.1:p.Glu176=
XR_243204.1:n.609G=
XR_931756.1:n.715G=
XM_017021934.2:c.580G=	XP_016877423.1:p.Glu194=
XM_017021935.2:c.15G=	XP_016877424.1:p.Trp5=
XM_017021936.2:c.15G=	XP_016877425.1:p.Trp5=
XR_001751098.2:n.727G=
XR_931756.3:n.728G=
NM_001307952.2:c.580G=	NP_001294881.1:p.Glu194=
NM_178232.4:c.394G= MANE Select	NP_839946.1:p.Glu132=