Canonical Allele Identifier: CA492066333

Gene: HAPLN3

Linked Data

• MyVariant Identifiers: chr15:g.89424609G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.88881378G>A , CM000677.2:g.88881378G>A	GRCh38
NC_000015.9:g.89424609G>A , CM000677.1:g.89424609G>A	GRCh37
NC_000015.8:g.87225613G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359595.8:c.472C>T MANE Select	ENSP00000352606.4:p.Leu158=
ENST00000359595.7:c.472C>T	ENSP00000352606.3:p.Leu158=
ENST00000558770.5:c.472C>T	ENSP00000456458.1:p.Leu158=
ENST00000562281.1:c.472C>T	ENSP00000456985.1:p.Leu158=
ENST00000562889.5:c.658C>T	ENSP00000457180.1:p.Leu220=
ENST00000563808.1:n.574C>T
NM_001307952.1:c.658C>T	NP_001294881.1:p.Leu220=
NM_178232.2:c.472C>T	NP_839946.1:p.Leu158=
NM_178232.3:c.472C>T	NP_839946.1:p.Leu158=
XM_011521261.1:c.604C>T	XP_011519563.1:p.Leu202=
XR_243204.1:n.687C>T
XR_931756.1:n.793C>T
XM_017021934.2:c.658C>T	XP_016877423.1:p.Leu220=
XM_017021935.2:c.93C>T	XP_016877424.1:p.Val31=
XM_017021936.2:c.93C>T	XP_016877425.1:p.Val31=
XR_001751098.2:n.805C>T
XR_931756.3:n.806C>T
NM_001307952.2:c.658C>T	NP_001294881.1:p.Leu220=
NM_178232.4:c.472C>T MANE Select	NP_839946.1:p.Leu158=