Canonical Allele Identifier: CA2194345932

Gene: HAPLN3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.88881399C= , CM000677.2:g.88881399C=	GRCh38
NC_000015.9:g.89424630C= , CM000677.1:g.89424630C=	GRCh37
NC_000015.8:g.87225634C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359595.8:c.451G= MANE Select	ENSP00000352606.4:p.Gly151=
ENST00000359595.7:c.451G=	ENSP00000352606.3:p.Gly151=
ENST00000558770.5:c.451G=	ENSP00000456458.1:p.Gly151=
ENST00000562281.1:c.451G=	ENSP00000456985.1:p.Gly151=
ENST00000562889.5:c.637G=	ENSP00000457180.1:p.Gly213=
ENST00000563808.1:n.553G=
NM_001307952.1:c.637G=	NP_001294881.1:p.Gly213=
NM_178232.2:c.451G=	NP_839946.1:p.Gly151=
NM_178232.3:c.451G=	NP_839946.1:p.Gly151=
XM_011521261.1:c.583G=	XP_011519563.1:p.Gly195=
XR_243204.1:n.666G=
XR_931756.1:n.772G=
XM_017021934.2:c.637G=	XP_016877423.1:p.Gly213=
XM_017021935.2:c.72G=	XP_016877424.1:p.Thr24=
XM_017021936.2:c.72G=	XP_016877425.1:p.Thr24=
XR_001751098.2:n.784G=
XR_931756.3:n.785G=
NM_001307952.2:c.637G=	NP_001294881.1:p.Gly213=
NM_178232.4:c.451G= MANE Select	NP_839946.1:p.Gly151=