Canonical Allele Identifier: CA2194346662

Gene: HAPLN3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.88881699C= , CM000677.2:g.88881699C=	GRCh38
NC_000015.9:g.89424930C= , CM000677.1:g.89424930C=	GRCh37
NC_000015.8:g.87225934C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359595.8:c.151G= MANE Select	ENSP00000352606.4:p.Val51=
ENST00000359595.7:c.151G=	ENSP00000352606.3:p.Val51=
ENST00000558770.5:c.151G=	ENSP00000456458.1:p.Val51=
ENST00000562281.1:c.151G=	ENSP00000456985.1:p.Val51=
ENST00000562889.5:c.337G=	ENSP00000457180.1:p.Val113=
ENST00000563808.1:n.253G=
NM_001307952.1:c.337G=	NP_001294881.1:p.Val113=
NM_178232.2:c.151G=	NP_839946.1:p.Val51=
NM_178232.3:c.151G=	NP_839946.1:p.Val51=
XM_011521261.1:c.283G=	XP_011519563.1:p.Val95=
XR_243204.1:n.366G=
XR_931756.1:n.472G=
XM_017021934.2:c.337G=	XP_016877423.1:p.Val113=
XM_017021935.2:c.-229G=	XP_016877424.1:n.-229G=
XM_017021936.2:c.-229G=	XP_016877425.1:n.-229G=
XR_001751098.2:n.484G=
XR_931756.3:n.485G=
NM_001307952.2:c.337G=	NP_001294881.1:p.Val113=
NM_178232.4:c.151G= MANE Select	NP_839946.1:p.Val51=