Canonical Allele Identifier: CA393733518

Gene: HAPLN3

Linked Data

• dbSNP Id: rs1387745263
• MyVariant Identifiers: chr15:g.89424650T>A (hg19) ; chr15:g.88881419T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.88881419T>A , CM000677.2:g.88881419T>A	GRCh38
NC_000015.9:g.89424650T>A , CM000677.1:g.89424650T>A	GRCh37
NC_000015.8:g.87225654T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359595.8:c.431A>T MANE Select	ENSP00000352606.4:p.Tyr144Phe
ENST00000359595.7:c.431A>T	ENSP00000352606.3:p.Tyr144Phe
ENST00000558770.5:c.431A>T	ENSP00000456458.1:p.Tyr144Phe
ENST00000562281.1:c.431A>T	ENSP00000456985.1:p.Tyr144Phe
ENST00000562889.5:c.617A>T	ENSP00000457180.1:p.Tyr206Phe
ENST00000563808.1:n.533A>T
NM_001307952.1:c.617A>T	NP_001294881.1:p.Tyr206Phe
NM_178232.2:c.431A>T	NP_839946.1:p.Tyr144Phe
NM_178232.3:c.431A>T	NP_839946.1:p.Tyr144Phe
XM_011521261.1:c.563A>T	XP_011519563.1:p.Tyr188Phe
XR_243204.1:n.646A>T
XR_931756.1:n.752A>T
XM_017021934.2:c.617A>T	XP_016877423.1:p.Tyr206Phe
XM_017021935.2:c.52A>T	XP_016877424.1:p.Thr18Ser
XM_017021936.2:c.52A>T	XP_016877425.1:p.Thr18Ser
XR_001751098.2:n.764A>T
XR_931756.3:n.765A>T
NM_001307952.2:c.617A>T	NP_001294881.1:p.Tyr206Phe
NM_178232.4:c.431A>T MANE Select	NP_839946.1:p.Tyr144Phe