Canonical Allele Identifier: CA393734005

Gene: HAPLN3

Linked Data

• MyVariant Identifiers: chr15:g.89424899T>A (hg19) ; chr15:g.88881668T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.88881668T>A , CM000677.2:g.88881668T>A	GRCh38
NC_000015.9:g.89424899T>A , CM000677.1:g.89424899T>A	GRCh37
NC_000015.8:g.87225903T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359595.8:c.182A>T MANE Select	ENSP00000352606.4:p.Tyr61Phe
ENST00000359595.7:c.182A>T	ENSP00000352606.3:p.Tyr61Phe
ENST00000558770.5:c.182A>T	ENSP00000456458.1:p.Tyr61Phe
ENST00000562281.1:c.182A>T	ENSP00000456985.1:p.Tyr61Phe
ENST00000562889.5:c.368A>T	ENSP00000457180.1:p.Tyr123Phe
ENST00000563808.1:n.284A>T
NM_001307952.1:c.368A>T	NP_001294881.1:p.Tyr123Phe
NM_178232.2:c.182A>T	NP_839946.1:p.Tyr61Phe
NM_178232.3:c.182A>T	NP_839946.1:p.Tyr61Phe
XM_011521261.1:c.314A>T	XP_011519563.1:p.Tyr105Phe
XR_243204.1:n.397A>T
XR_931756.1:n.503A>T
XM_017021934.2:c.368A>T	XP_016877423.1:p.Tyr123Phe
XM_017021935.2:c.-198A>T	XP_016877424.1:n.-198A>T
XM_017021936.2:c.-198A>T	XP_016877425.1:n.-198A>T
XR_001751098.2:n.515A>T
XR_931756.3:n.516A>T
NM_001307952.2:c.368A>T	NP_001294881.1:p.Tyr123Phe
NM_178232.4:c.182A>T MANE Select	NP_839946.1:p.Tyr61Phe