Canonical Allele Identifier: CA393734048

Gene: HAPLN3

Linked Data

• gnomAD v4: 15-88881687-C-A
• MyVariant Identifiers: chr15:g.89424918C>A (hg19) ; chr15:g.88881687C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.88881687C>A , CM000677.2:g.88881687C>A	GRCh38
NC_000015.9:g.89424918C>A , CM000677.1:g.89424918C>A	GRCh37
NC_000015.8:g.87225922C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359595.8:c.163G>T MANE Select	ENSP00000352606.4:p.Glu55Ter
ENST00000359595.7:c.163G>T	ENSP00000352606.3:p.Glu55Ter
ENST00000558770.5:c.163G>T	ENSP00000456458.1:p.Glu55Ter
ENST00000562281.1:c.163G>T	ENSP00000456985.1:p.Glu55Ter
ENST00000562889.5:c.349G>T	ENSP00000457180.1:p.Glu117Ter
ENST00000563808.1:n.265G>T
NM_001307952.1:c.349G>T	NP_001294881.1:p.Glu117Ter
NM_178232.2:c.163G>T	NP_839946.1:p.Glu55Ter
NM_178232.3:c.163G>T	NP_839946.1:p.Glu55Ter
XM_011521261.1:c.295G>T	XP_011519563.1:p.Glu99Ter
XR_243204.1:n.378G>T
XR_931756.1:n.484G>T
XM_017021934.2:c.349G>T	XP_016877423.1:p.Glu117Ter
XM_017021935.2:c.-217G>T	XP_016877424.1:n.-217G>T
XM_017021936.2:c.-217G>T	XP_016877425.1:n.-217G>T
XR_001751098.2:n.496G>T
XR_931756.3:n.497G>T
NM_001307952.2:c.349G>T	NP_001294881.1:p.Glu117Ter
NM_178232.4:c.163G>T MANE Select	NP_839946.1:p.Glu55Ter