Canonical Allele Identifier: CA393734128

Gene: HAPLN3

Linked Data

• MyVariant Identifiers: chr15:g.89424957C>T (hg19) ; chr15:g.88881726C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.88881726C>T , CM000677.2:g.88881726C>T	GRCh38
NC_000015.9:g.89424957C>T , CM000677.1:g.89424957C>T	GRCh37
NC_000015.8:g.87225961C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359595.8:c.125-1G>A MANE Select	ENSP00000352606.4:n.125-1G>A
ENST00000359595.7:c.125-1G>A	ENSP00000352606.3:n.125-1G>A
ENST00000558770.5:c.125-1G>A	ENSP00000456458.1:n.125-1G>A
ENST00000562281.1:c.125-1G>A	ENSP00000456985.1:n.125-1G>A
ENST00000562889.5:c.311-1G>A	ENSP00000457180.1:n.311-1G>A
ENST00000563808.1:n.227-1G>A
NM_001307952.1:c.311-1G>A	NP_001294881.1:n.311-1G>A
NM_178232.2:c.125-1G>A	NP_839946.1:n.125-1G>A
NM_178232.3:c.125-1G>A	NP_839946.1:n.125-1G>A
XM_011521261.1:c.257-1G>A	XP_011519563.1:n.257-1G>A
XR_243204.1:n.340-1G>A
XR_931756.1:n.446-1G>A
XM_017021934.2:c.311-1G>A	XP_016877423.1:n.311-1G>A
XM_017021935.2:c.-255-1G>A	XP_016877424.1:n.-255-1G>A
XM_017021936.2:c.-255-1G>A	XP_016877425.1:n.-255-1G>A
XR_001751098.2:n.458-1G>A
XR_931756.3:n.459-1G>A
NM_001307952.2:c.311-1G>A	NP_001294881.1:n.311-1G>A
NM_178232.4:c.125-1G>A MANE Select	NP_839946.1:n.125-1G>A