Canonical Allele Identifier: CA393733467

Gene: HAPLN3

Linked Data

• dbSNP Id: rs1567200816
• MyVariant Identifiers: chr15:g.89424627G>T (hg19) ; chr15:g.88881396G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.88881396G>T , CM000677.2:g.88881396G>T	GRCh38
NC_000015.9:g.89424627G>T , CM000677.1:g.89424627G>T	GRCh37
NC_000015.8:g.87225631G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359595.8:c.454C>A MANE Select	ENSP00000352606.4:p.Leu152Met
ENST00000359595.7:c.454C>A	ENSP00000352606.3:p.Leu152Met
ENST00000558770.5:c.454C>A	ENSP00000456458.1:p.Leu152Met
ENST00000562281.1:c.454C>A	ENSP00000456985.1:p.Leu152Met
ENST00000562889.5:c.640C>A	ENSP00000457180.1:p.Leu214Met
ENST00000563808.1:n.556C>A
NM_001307952.1:c.640C>A	NP_001294881.1:p.Leu214Met
NM_178232.2:c.454C>A	NP_839946.1:p.Leu152Met
NM_178232.3:c.454C>A	NP_839946.1:p.Leu152Met
XM_011521261.1:c.586C>A	XP_011519563.1:p.Leu196Met
XR_243204.1:n.669C>A
XR_931756.1:n.775C>A
XM_017021934.2:c.640C>A	XP_016877423.1:p.Leu214Met
XM_017021935.2:c.75C>A	XP_016877424.1:p.Gly25=
XM_017021936.2:c.75C>A	XP_016877425.1:p.Gly25=
XR_001751098.2:n.787C>A
XR_931756.3:n.788C>A
NM_001307952.2:c.640C>A	NP_001294881.1:p.Leu214Met
NM_178232.4:c.454C>A MANE Select	NP_839946.1:p.Leu152Met