Canonical Allele Identifier: CA2194345936

Gene: HAPLN3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.88881400G= , CM000677.2:g.88881400G=	GRCh38
NC_000015.9:g.89424631G= , CM000677.1:g.89424631G=	GRCh37
NC_000015.8:g.87225635G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359595.8:c.450C= MANE Select	ENSP00000352606.4:p.Asp150=
ENST00000359595.7:c.450C=	ENSP00000352606.3:p.Asp150=
ENST00000558770.5:c.450C=	ENSP00000456458.1:p.Asp150=
ENST00000562281.1:c.450C=	ENSP00000456985.1:p.Asp150=
ENST00000562889.5:c.636C=	ENSP00000457180.1:p.Asp212=
ENST00000563808.1:n.552C=
NM_001307952.1:c.636C=	NP_001294881.1:p.Asp212=
NM_178232.2:c.450C=	NP_839946.1:p.Asp150=
NM_178232.3:c.450C=	NP_839946.1:p.Asp150=
XM_011521261.1:c.582C=	XP_011519563.1:p.Asp194=
XR_243204.1:n.665C=
XR_931756.1:n.771C=
XM_017021934.2:c.636C=	XP_016877423.1:p.Asp212=
XM_017021935.2:c.71C=	XP_016877424.1:p.Thr24=
XM_017021936.2:c.71C=	XP_016877425.1:p.Thr24=
XR_001751098.2:n.783C=
XR_931756.3:n.784C=
NM_001307952.2:c.636C=	NP_001294881.1:p.Asp212=
NM_178232.4:c.450C= MANE Select	NP_839946.1:p.Asp150=