Canonical Allele Identifier: CA492288601

Gene: HAPLN3

Linked Data

• MyVariant Identifiers: chr15:g.89424913C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.88881682C>T , CM000677.2:g.88881682C>T	GRCh38
NC_000015.9:g.89424913C>T , CM000677.1:g.89424913C>T	GRCh37
NC_000015.8:g.87225917C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359595.8:c.168G>A MANE Select	ENSP00000352606.4:p.Glu56=
ENST00000359595.7:c.168G>A	ENSP00000352606.3:p.Glu56=
ENST00000558770.5:c.168G>A	ENSP00000456458.1:p.Glu56=
ENST00000562281.1:c.168G>A	ENSP00000456985.1:p.Glu56=
ENST00000562889.5:c.354G>A	ENSP00000457180.1:p.Glu118=
ENST00000563808.1:n.270G>A
NM_001307952.1:c.354G>A	NP_001294881.1:p.Glu118=
NM_178232.2:c.168G>A	NP_839946.1:p.Glu56=
NM_178232.3:c.168G>A	NP_839946.1:p.Glu56=
XM_011521261.1:c.300G>A	XP_011519563.1:p.Glu100=
XR_243204.1:n.383G>A
XR_931756.1:n.489G>A
XM_017021934.2:c.354G>A	XP_016877423.1:p.Glu118=
XM_017021935.2:c.-212G>A	XP_016877424.1:n.-212G>A
XM_017021936.2:c.-212G>A	XP_016877425.1:n.-212G>A
XR_001751098.2:n.501G>A
XR_931756.3:n.502G>A
NM_001307952.2:c.354G>A	NP_001294881.1:p.Glu118=
NM_178232.4:c.168G>A MANE Select	NP_839946.1:p.Glu56=