Canonical Allele Identifier: CA7721147

Gene: HAPLN3

Linked Data

• dbSNP Id: rs779912934
• ExAC: 15:89424892 C / A
• gnomAD v2: 15-89424892-C-A
• gnomAD v3: 15-88881661-C-A
• gnomAD v4: 15-88881661-C-A
• MyVariant Identifiers: chr15:g.89424892C>A (hg19) ; chr15:g.88881661C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.88881661C>A , CM000677.2:g.88881661C>A	GRCh38
NC_000015.9:g.89424892C>A , CM000677.1:g.89424892C>A	GRCh37
NC_000015.8:g.87225896C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359595.8:c.189G>T MANE Select	ENSP00000352606.4:p.Gly63=
ENST00000359595.7:c.189G>T	ENSP00000352606.3:p.Gly63=
ENST00000558770.5:c.189G>T	ENSP00000456458.1:p.Gly63=
ENST00000562281.1:c.189G>T	ENSP00000456985.1:p.Gly63=
ENST00000562889.5:c.375G>T	ENSP00000457180.1:p.Gly125=
ENST00000563808.1:n.291G>T
NM_001307952.1:c.375G>T	NP_001294881.1:p.Gly125=
NM_178232.2:c.189G>T	NP_839946.1:p.Gly63=
NM_178232.3:c.189G>T	NP_839946.1:p.Gly63=
XM_011521261.1:c.321G>T	XP_011519563.1:p.Gly107=
XR_243204.1:n.404G>T
XR_931756.1:n.510G>T
XM_017021934.2:c.375G>T	XP_016877423.1:p.Gly125=
XM_017021935.2:c.-191G>T	XP_016877424.1:n.-191G>T
XM_017021936.2:c.-191G>T	XP_016877425.1:n.-191G>T
XR_001751098.2:n.522G>T
XR_931756.3:n.523G>T
NM_001307952.2:c.375G>T	NP_001294881.1:p.Gly125=
NM_178232.4:c.189G>T MANE Select	NP_839946.1:p.Gly63=