Canonical Allele Identifier: CA2194346234

Gene: HAPLN3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.88881540C= , CM000677.2:g.88881540C=	GRCh38
NC_000015.9:g.89424771C= , CM000677.1:g.89424771C=	GRCh37
NC_000015.8:g.87225775C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000359595.8:c.310G= MANE Select	ENSP00000352606.4:p.Ala104=
ENST00000359595.7:c.310G=	ENSP00000352606.3:p.Ala104=
ENST00000558770.5:c.310G=	ENSP00000456458.1:p.Ala104=
ENST00000562281.1:c.310G=	ENSP00000456985.1:p.Ala104=
ENST00000562889.5:c.496G=	ENSP00000457180.1:p.Ala166=
ENST00000563808.1:n.412G=
NM_001307952.1:c.496G=	NP_001294881.1:p.Ala166=
NM_178232.2:c.310G=	NP_839946.1:p.Ala104=
NM_178232.3:c.310G=	NP_839946.1:p.Ala104=
XM_011521261.1:c.442G=	XP_011519563.1:p.Ala148=
XR_243204.1:n.525G=
XR_931756.1:n.631G=
XM_017021934.2:c.496G=	XP_016877423.1:p.Ala166=
XM_017021935.2:c.-70G=	XP_016877424.1:n.-70G=
XM_017021936.2:c.-70G=	XP_016877425.1:n.-70G=
XR_001751098.2:n.643G=
XR_931756.3:n.644G=
NM_001307952.2:c.496G=	NP_001294881.1:p.Ala166=
NM_178232.4:c.310G= MANE Select	NP_839946.1:p.Ala104=