Canonical Allele Identifier: CA393733513

Gene: HAPLN3

Linked Data

• COSMIC: COSM4057739
• MyVariant Identifiers: chr15:g.89424648G>T (hg19) ; chr15:g.88881417G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.88881417G>T , CM000677.2:g.88881417G>T	GRCh38
NC_000015.9:g.89424648G>T , CM000677.1:g.89424648G>T	GRCh37
NC_000015.8:g.87225652G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359595.8:c.433C>A MANE Select	ENSP00000352606.4:p.Arg145Ser
ENST00000359595.7:c.433C>A	ENSP00000352606.3:p.Arg145Ser
ENST00000558770.5:c.433C>A	ENSP00000456458.1:p.Arg145Ser
ENST00000562281.1:c.433C>A	ENSP00000456985.1:p.Arg145Ser
ENST00000562889.5:c.619C>A	ENSP00000457180.1:p.Arg207Ser
ENST00000563808.1:n.535C>A
NM_001307952.1:c.619C>A	NP_001294881.1:p.Arg207Ser
NM_178232.2:c.433C>A	NP_839946.1:p.Arg145Ser
NM_178232.3:c.433C>A	NP_839946.1:p.Arg145Ser
XM_011521261.1:c.565C>A	XP_011519563.1:p.Arg189Ser
XR_243204.1:n.648C>A
XR_931756.1:n.754C>A
XM_017021934.2:c.619C>A	XP_016877423.1:p.Arg207Ser
XM_017021935.2:c.54C>A	XP_016877424.1:p.Thr18=
XM_017021936.2:c.54C>A	XP_016877425.1:p.Thr18=
XR_001751098.2:n.766C>A
XR_931756.3:n.767C>A
NM_001307952.2:c.619C>A	NP_001294881.1:p.Arg207Ser
NM_178232.4:c.433C>A MANE Select	NP_839946.1:p.Arg145Ser