Canonical Allele Identifier: CA492066334

Gene: HAPLN3

Linked Data

• dbSNP Id: rs760242665
• MyVariant Identifiers: chr15:g.89424610A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.88881379A>C , CM000677.2:g.88881379A>C	GRCh38
NC_000015.9:g.89424610A>C , CM000677.1:g.89424610A>C	GRCh37
NC_000015.8:g.87225614A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359595.8:c.471T>G MANE Select	ENSP00000352606.4:p.Gly157=
ENST00000359595.7:c.471T>G	ENSP00000352606.3:p.Gly157=
ENST00000558770.5:c.471T>G	ENSP00000456458.1:p.Gly157=
ENST00000562281.1:c.471T>G	ENSP00000456985.1:p.Gly157=
ENST00000562889.5:c.657T>G	ENSP00000457180.1:p.Gly219=
ENST00000563808.1:n.573T>G
NM_001307952.1:c.657T>G	NP_001294881.1:p.Gly219=
NM_178232.2:c.471T>G	NP_839946.1:p.Gly157=
NM_178232.3:c.471T>G	NP_839946.1:p.Gly157=
XM_011521261.1:c.603T>G	XP_011519563.1:p.Gly201=
XR_243204.1:n.686T>G
XR_931756.1:n.792T>G
XM_017021934.2:c.657T>G	XP_016877423.1:p.Gly219=
XM_017021935.2:c.92T>G	XP_016877424.1:p.Val31Gly
XM_017021936.2:c.92T>G	XP_016877425.1:p.Val31Gly
XR_001751098.2:n.804T>G
XR_931756.3:n.805T>G
NM_001307952.2:c.657T>G	NP_001294881.1:p.Gly219=
NM_178232.4:c.471T>G MANE Select	NP_839946.1:p.Gly157=