Canonical Allele Identifier: CA7721115

Gene: HAPLN3

Linked Data

• dbSNP Id: rs764742514
• ExAC: 15:89424827 C / G
• gnomAD v2: 15-89424827-C-G
• gnomAD v4: 15-88881596-C-G
• MyVariant Identifiers: chr15:g.89424827C>G (hg19) ; chr15:g.88881596C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.88881596C>G , CM000677.2:g.88881596C>G	GRCh38
NC_000015.9:g.89424827C>G , CM000677.1:g.89424827C>G	GRCh37
NC_000015.8:g.87225831C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359595.8:c.254G>C MANE Select	ENSP00000352606.4:p.Arg85Pro
ENST00000359595.7:c.254G>C	ENSP00000352606.3:p.Arg85Pro
ENST00000558770.5:c.254G>C	ENSP00000456458.1:p.Arg85Pro
ENST00000562281.1:c.254G>C	ENSP00000456985.1:p.Arg85Pro
ENST00000562889.5:c.440G>C	ENSP00000457180.1:p.Arg147Pro
ENST00000563808.1:n.356G>C
NM_001307952.1:c.440G>C	NP_001294881.1:p.Arg147Pro
NM_178232.2:c.254G>C	NP_839946.1:p.Arg85Pro
NM_178232.3:c.254G>C	NP_839946.1:p.Arg85Pro
XM_011521261.1:c.386G>C	XP_011519563.1:p.Arg129Pro
XR_243204.1:n.469G>C
XR_931756.1:n.575G>C
XM_017021934.2:c.440G>C	XP_016877423.1:p.Arg147Pro
XM_017021935.2:c.-126G>C	XP_016877424.1:n.-126G>C
XM_017021936.2:c.-126G>C	XP_016877425.1:n.-126G>C
XR_001751098.2:n.587G>C
XR_931756.3:n.588G>C
NM_001307952.2:c.440G>C	NP_001294881.1:p.Arg147Pro
NM_178232.4:c.254G>C MANE Select	NP_839946.1:p.Arg85Pro