Canonical Allele Identifier: CA2559599374

Gene: HAPLN3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.88881195_88881196insAAA , CM000677.2:g.88881195_88881196insAAA	GRCh38
NC_000015.9:g.89424426_89424427insAAA , CM000677.1:g.89424426_89424427insAAA	GRCh37
NC_000015.8:g.87225430_87225431insAAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359595.8:c.493+161_493+162insTTT MANE Select	ENSP00000352606.4:n.493+161_493+162insTTT
ENST00000359595.7:c.493+161_493+162insTTT	ENSP00000352606.3:n.493+161_493+162insTTT
ENST00000558770.5:c.493+161_493+162insTTT	ENSP00000456458.1:n.493+161_493+162insTTT
ENST00000562281.1:c.493+161_493+162insTTT	ENSP00000456985.1:n.493+161_493+162insTTT
ENST00000562889.5:c.679+161_679+162insTTT	ENSP00000457180.1:n.679+161_679+162insTTT
ENST00000563808.1:n.756_757insTTT
NM_001307952.1:c.679+161_679+162insTTT	NP_001294881.1:n.679+161_679+162insTTT
NM_178232.2:c.493+161_493+162insTTT	NP_839946.1:n.493+161_493+162insTTT
NM_178232.3:c.493+161_493+162insTTT	NP_839946.1:n.493+161_493+162insTTT
XM_011521261.1:c.625+161_625+162insTTT	XP_011519563.1:n.625+161_625+162insTTT
XR_243204.1:n.708+161_708+162insTTT
XR_931756.1:n.814+161_814+162insTTT
XM_017021934.2:c.679+161_679+162insTTT	XP_016877423.1:n.679+161_679+162insTTT
XM_017021935.2:c.114+161_114+162insTTT	XP_016877424.1:n.114+161_114+162insTTT
XM_017021936.2:c.114+161_114+162insTTT	XP_016877425.1:n.114+161_114+162insTTT
XR_001751098.2:n.826+161_826+162insTTT
XR_931756.3:n.827+161_827+162insTTT
NM_001307952.2:c.679+161_679+162insTTT	NP_001294881.1:n.679+161_679+162insTTT
NM_178232.4:c.493+161_493+162insTTT MANE Select	NP_839946.1:n.493+161_493+162insTTT