Canonical Allele Identifier: CA393733521

Gene: HAPLN3

Linked Data

• MyVariant Identifiers: chr15:g.89424653C>A (hg19) ; chr15:g.88881422C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.88881422C>A , CM000677.2:g.88881422C>A	GRCh38
NC_000015.9:g.89424653C>A , CM000677.1:g.89424653C>A	GRCh37
NC_000015.8:g.87225657C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359595.8:c.428G>T MANE Select	ENSP00000352606.4:p.Arg143Leu
ENST00000359595.7:c.428G>T	ENSP00000352606.3:p.Arg143Leu
ENST00000558770.5:c.428G>T	ENSP00000456458.1:p.Arg143Leu
ENST00000562281.1:c.428G>T	ENSP00000456985.1:p.Arg143Leu
ENST00000562889.5:c.614G>T	ENSP00000457180.1:p.Arg205Leu
ENST00000563808.1:n.530G>T
NM_001307952.1:c.614G>T	NP_001294881.1:p.Arg205Leu
NM_178232.2:c.428G>T	NP_839946.1:p.Arg143Leu
NM_178232.3:c.428G>T	NP_839946.1:p.Arg143Leu
XM_011521261.1:c.560G>T	XP_011519563.1:p.Arg187Leu
XR_243204.1:n.643G>T
XR_931756.1:n.749G>T
XM_017021934.2:c.614G>T	XP_016877423.1:p.Arg205Leu
XM_017021935.2:c.49G>T	XP_016877424.1:p.Val17Phe
XM_017021936.2:c.49G>T	XP_016877425.1:p.Val17Phe
XR_001751098.2:n.761G>T
XR_931756.3:n.762G>T
NM_001307952.2:c.614G>T	NP_001294881.1:p.Arg205Leu
NM_178232.4:c.428G>T MANE Select	NP_839946.1:p.Arg143Leu