Canonical Allele Identifier: CA7721067
Gene: HAPLN3 HGNC NCBI

Linked Data

dbSNP Id: rs761651342

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.88881434T>C , CM000677.2:g.88881434T>C GRCh38
NC_000015.9:g.89424665T>C , CM000677.1:g.89424665T>C GRCh37
NC_000015.8:g.87225669T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000359595.8:c.416A>G MANE Select ENSP00000352606.4:p.Glu139Gly
ENST00000359595.7:c.416A>G ENSP00000352606.3:p.Glu139Gly
ENST00000558770.5:c.416A>G ENSP00000456458.1:p.Glu139Gly
ENST00000562281.1:c.416A>G ENSP00000456985.1:p.Glu139Gly
ENST00000562889.5:c.602A>G ENSP00000457180.1:p.Glu201Gly
ENST00000563808.1:n.518A>G
NM_001307952.1:c.602A>G NP_001294881.1:p.Glu201Gly
NM_178232.2:c.416A>G NP_839946.1:p.Glu139Gly
NM_178232.3:c.416A>G NP_839946.1:p.Glu139Gly
XM_011521261.1:c.548A>G XP_011519563.1:p.Glu183Gly
XR_243204.1:n.631A>G
XR_931756.1:n.737A>G
XM_017021934.2:c.602A>G XP_016877423.1:p.Glu201Gly
XM_017021935.2:c.37A>G XP_016877424.1:p.Arg13Gly
XM_017021936.2:c.37A>G XP_016877425.1:p.Arg13Gly
XR_001751098.2:n.749A>G
XR_931756.3:n.750A>G
NM_001307952.2:c.602A>G NP_001294881.1:p.Glu201Gly
NM_178232.4:c.416A>G MANE Select NP_839946.1:p.Glu139Gly