Canonical Allele Identifier: CA2630224016

Gene: HAPLN3

Linked Data

• gnomAD v4: 15-88881202-T-TTTA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.88881202_88881203insTTA , CM000677.2:g.88881202_88881203insTTA	GRCh38
NC_000015.9:g.89424433_89424434insTTA , CM000677.1:g.89424433_89424434insTTA	GRCh37
NC_000015.8:g.87225437_87225438insTTA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359595.8:c.493+154_493+155insTAA MANE Select	ENSP00000352606.4:n.493+154_493+155insTAA
ENST00000359595.7:c.493+154_493+155insTAA	ENSP00000352606.3:n.493+154_493+155insTAA
ENST00000558770.5:c.493+154_493+155insTAA	ENSP00000456458.1:n.493+154_493+155insTAA
ENST00000562281.1:c.493+154_493+155insTAA	ENSP00000456985.1:n.493+154_493+155insTAA
ENST00000562889.5:c.679+154_679+155insTAA	ENSP00000457180.1:n.679+154_679+155insTAA
ENST00000563808.1:n.749_750insTAA
NM_001307952.1:c.679+154_679+155insTAA	NP_001294881.1:n.679+154_679+155insTAA
NM_178232.2:c.493+154_493+155insTAA	NP_839946.1:n.493+154_493+155insTAA
NM_178232.3:c.493+154_493+155insTAA	NP_839946.1:n.493+154_493+155insTAA
XM_011521261.1:c.625+154_625+155insTAA	XP_011519563.1:n.625+154_625+155insTAA
XR_243204.1:n.708+154_708+155insTAA
XR_931756.1:n.814+154_814+155insTAA
XM_017021934.2:c.679+154_679+155insTAA	XP_016877423.1:n.679+154_679+155insTAA
XM_017021935.2:c.114+154_114+155insTAA	XP_016877424.1:n.114+154_114+155insTAA
XM_017021936.2:c.114+154_114+155insTAA	XP_016877425.1:n.114+154_114+155insTAA
XR_001751098.2:n.826+154_826+155insTAA
XR_931756.3:n.827+154_827+155insTAA
NM_001307952.2:c.679+154_679+155insTAA	NP_001294881.1:n.679+154_679+155insTAA
NM_178232.4:c.493+154_493+155insTAA MANE Select	NP_839946.1:n.493+154_493+155insTAA