Canonical Allele Identifier: CA2194346650

Gene: HAPLN3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.88881690G= , CM000677.2:g.88881690G=	GRCh38
NC_000015.9:g.89424921G= , CM000677.1:g.89424921G=	GRCh37
NC_000015.8:g.87225925G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359595.8:c.160C= MANE Select	ENSP00000352606.4:p.Pro54=
ENST00000359595.7:c.160C=	ENSP00000352606.3:p.Pro54=
ENST00000558770.5:c.160C=	ENSP00000456458.1:p.Pro54=
ENST00000562281.1:c.160C=	ENSP00000456985.1:p.Pro54=
ENST00000562889.5:c.346C=	ENSP00000457180.1:p.Pro116=
ENST00000563808.1:n.262C=
NM_001307952.1:c.346C=	NP_001294881.1:p.Pro116=
NM_178232.2:c.160C=	NP_839946.1:p.Pro54=
NM_178232.3:c.160C=	NP_839946.1:p.Pro54=
XM_011521261.1:c.292C=	XP_011519563.1:p.Pro98=
XR_243204.1:n.375C=
XR_931756.1:n.481C=
XM_017021934.2:c.346C=	XP_016877423.1:p.Pro116=
XM_017021935.2:c.-220C=	XP_016877424.1:n.-220C=
XM_017021936.2:c.-220C=	XP_016877425.1:n.-220C=
XR_001751098.2:n.493C=
XR_931756.3:n.494C=
NM_001307952.2:c.346C=	NP_001294881.1:p.Pro116=
NM_178232.4:c.160C= MANE Select	NP_839946.1:p.Pro54=