Canonical Allele Identifier: CA7721112
Gene: HAPLN3 HGNC NCBI

Linked Data

dbSNP Id: rs776092317

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.88881589T>C , CM000677.2:g.88881589T>C GRCh38
NC_000015.9:g.89424820T>C , CM000677.1:g.89424820T>C GRCh37
NC_000015.8:g.87225824T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000359595.8:c.261A>G MANE Select ENSP00000352606.4:p.Lys87=
ENST00000359595.7:c.261A>G ENSP00000352606.3:p.Lys87=
ENST00000558770.5:c.261A>G ENSP00000456458.1:p.Lys87=
ENST00000562281.1:c.261A>G ENSP00000456985.1:p.Lys87=
ENST00000562889.5:c.447A>G ENSP00000457180.1:p.Lys149=
ENST00000563808.1:n.363A>G
NM_001307952.1:c.447A>G NP_001294881.1:p.Lys149=
NM_178232.2:c.261A>G NP_839946.1:p.Lys87=
NM_178232.3:c.261A>G NP_839946.1:p.Lys87=
XM_011521261.1:c.393A>G XP_011519563.1:p.Lys131=
XR_243204.1:n.476A>G
XR_931756.1:n.582A>G
XM_017021934.2:c.447A>G XP_016877423.1:p.Lys149=
XM_017021935.2:c.-119A>G XP_016877424.1:n.-119A>G
XM_017021936.2:c.-119A>G XP_016877425.1:n.-119A>G
XR_001751098.2:n.594A>G
XR_931756.3:n.595A>G
NM_001307952.2:c.447A>G NP_001294881.1:p.Lys149=
NM_178232.4:c.261A>G MANE Select NP_839946.1:p.Lys87=