Canonical Allele Identifier: CA393733716

Gene: HAPLN3

Linked Data

• MyVariant Identifiers: chr15:g.89424750A>G (hg19) ; chr15:g.88881519A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.88881519A>G , CM000677.2:g.88881519A>G	GRCh38
NC_000015.9:g.89424750A>G , CM000677.1:g.89424750A>G	GRCh37
NC_000015.8:g.87225754A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359595.8:c.331T>C MANE Select	ENSP00000352606.4:p.Ser111Pro
ENST00000359595.7:c.331T>C	ENSP00000352606.3:p.Ser111Pro
ENST00000558770.5:c.331T>C	ENSP00000456458.1:p.Ser111Pro
ENST00000562281.1:c.331T>C	ENSP00000456985.1:p.Ser111Pro
ENST00000562889.5:c.517T>C	ENSP00000457180.1:p.Ser173Pro
ENST00000563808.1:n.433T>C
NM_001307952.1:c.517T>C	NP_001294881.1:p.Ser173Pro
NM_178232.2:c.331T>C	NP_839946.1:p.Ser111Pro
NM_178232.3:c.331T>C	NP_839946.1:p.Ser111Pro
XM_011521261.1:c.463T>C	XP_011519563.1:p.Ser155Pro
XR_243204.1:n.546T>C
XR_931756.1:n.652T>C
XM_017021934.2:c.517T>C	XP_016877423.1:p.Ser173Pro
XM_017021935.2:c.-49T>C	XP_016877424.1:n.-49T>C
XM_017021936.2:c.-49T>C	XP_016877425.1:n.-49T>C
XR_001751098.2:n.664T>C
XR_931756.3:n.665T>C
NM_001307952.2:c.517T>C	NP_001294881.1:p.Ser173Pro
NM_178232.4:c.331T>C MANE Select	NP_839946.1:p.Ser111Pro