Canonical Allele Identifier: CA492288528

Gene: HAPLN3

Linked Data

• MyVariant Identifiers: chr15:g.89424790T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.88881559T>A , CM000677.2:g.88881559T>A	GRCh38
NC_000015.9:g.89424790T>A , CM000677.1:g.89424790T>A	GRCh37
NC_000015.8:g.87225794T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359595.8:c.291A>T MANE Select	ENSP00000352606.4:p.Pro97=
ENST00000359595.7:c.291A>T	ENSP00000352606.3:p.Pro97=
ENST00000558770.5:c.291A>T	ENSP00000456458.1:p.Pro97=
ENST00000562281.1:c.291A>T	ENSP00000456985.1:p.Pro97=
ENST00000562889.5:c.477A>T	ENSP00000457180.1:p.Pro159=
ENST00000563808.1:n.393A>T
NM_001307952.1:c.477A>T	NP_001294881.1:p.Pro159=
NM_178232.2:c.291A>T	NP_839946.1:p.Pro97=
NM_178232.3:c.291A>T	NP_839946.1:p.Pro97=
XM_011521261.1:c.423A>T	XP_011519563.1:p.Pro141=
XR_243204.1:n.506A>T
XR_931756.1:n.612A>T
XM_017021934.2:c.477A>T	XP_016877423.1:p.Pro159=
XM_017021935.2:c.-89A>T	XP_016877424.1:n.-89A>T
XM_017021936.2:c.-89A>T	XP_016877425.1:n.-89A>T
XR_001751098.2:n.624A>T
XR_931756.3:n.625A>T
NM_001307952.2:c.477A>T	NP_001294881.1:p.Pro159=
NM_178232.4:c.291A>T MANE Select	NP_839946.1:p.Pro97=