Canonical Allele Identifier: CA492066308

Gene: HAPLN3

Linked Data

• gnomAD v4: 15-88881360-G-T
• MyVariant Identifiers: chr15:g.89424591G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.88881360G>T , CM000677.2:g.88881360G>T	GRCh38
NC_000015.9:g.89424591G>T , CM000677.1:g.89424591G>T	GRCh37
NC_000015.8:g.87225595G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359595.8:c.490C>A MANE Select	ENSP00000352606.4:p.Arg164=
ENST00000359595.7:c.490C>A	ENSP00000352606.3:p.Arg164=
ENST00000558770.5:c.490C>A	ENSP00000456458.1:p.Arg164=
ENST00000562281.1:c.490C>A	ENSP00000456985.1:p.Arg164=
ENST00000562889.5:c.676C>A	ENSP00000457180.1:p.Arg226=
ENST00000563808.1:n.592C>A
NM_001307952.1:c.676C>A	NP_001294881.1:p.Arg226=
NM_178232.2:c.490C>A	NP_839946.1:p.Arg164=
NM_178232.3:c.490C>A	NP_839946.1:p.Arg164=
XM_011521261.1:c.622C>A	XP_011519563.1:p.Arg208=
XR_243204.1:n.705C>A
XR_931756.1:n.811C>A
XM_017021934.2:c.676C>A	XP_016877423.1:p.Arg226=
XM_017021935.2:c.111C>A	XP_016877424.1:p.Cys37Ter
XM_017021936.2:c.111C>A	XP_016877425.1:p.Cys37Ter
XR_001751098.2:n.823C>A
XR_931756.3:n.824C>A
NM_001307952.2:c.676C>A	NP_001294881.1:p.Arg226=
NM_178232.4:c.490C>A MANE Select	NP_839946.1:p.Arg164=