Canonical Allele Identifier: CA116326
Gene: HYAL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3530
ClinVar RCV Id: RCV000003708
dbSNP Id: rs104893743
gnomAD v2: 3-50339586-C-T
gnomAD v3: 3-50302155-C-T
gnomAD v4: 3-50302155-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50302155C>T , CM000665.2:g.50302155C>T GRCh38
NC_000003.11:g.50339586C>T , CM000665.1:g.50339586C>T GRCh37
NC_000003.10:g.50314590C>T NCBI36
NG_009295.1:g.15227G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000395144.7:c.802G>A MANE Select ENSP00000378576.2:p.Glu268Lys
ENST00000266031.8:c.802G>A ENSP00000266031.4:p.Glu268Lys
ENST00000320295.12:c.802G>A ENSP00000346068.5:p.Glu268Lys
ENST00000395143.6:c.802G>A ENSP00000378575.2:p.Glu268Lys
ENST00000395144.6:c.802G>A ENSP00000378576.2:p.Glu268Lys
ENST00000447605.2:c.25G>A ENSP00000390149.2:p.Glu9Lys
ENST00000457214.6:c.256G>A ENSP00000393358.2:p.Glu86Lys
ENST00000618175.4:c.802G>A ENSP00000477903.1:p.Glu268Lys
NM_033159.3:c.802G>A NP_149349.2:p.Glu268Lys
NM_153281.1:c.802G>A NP_695013.1:p.Glu268Lys
NM_153282.2:c.802G>A NP_695014.1:p.Glu268Lys
NM_153283.2:c.256G>A NP_695015.1:p.Glu86Lys
NM_153285.2:c.25G>A NP_695017.1:p.Glu9Lys
NR_047690.1:n.1447G>A
XM_011533667.1:c.802G>A XP_011531969.1:p.Glu268Lys
XM_011533668.1:c.802G>A XP_011531970.1:p.Glu268Lys
XM_011533669.1:c.802G>A XP_011531971.1:p.Glu268Lys
XM_011533667.2:c.802G>A XP_011531969.1:p.Glu268Lys
XM_011533668.2:c.802G>A XP_011531970.1:p.Glu268Lys
XM_011533669.2:c.802G>A XP_011531971.1:p.Glu268Lys
NM_033159.4:c.802G>A MANE Select NP_149349.2:p.Glu268Lys
NM_153282.3:c.802G>A NP_695014.1:p.Glu268Lys
NM_153283.3:c.256G>A NP_695015.1:p.Glu86Lys
NM_153285.3:c.25G>A NP_695017.1:p.Glu9Lys
NR_047690.2:n.1420G>A
NM_153281.2:c.802G>A NP_695013.1:p.Glu268Lys