Canonical Allele Identifier: CA352891898

Gene: HYAL1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50302056C>T , CM000665.2:g.50302056C>T	GRCh38
NC_000003.11:g.50339487C>T , CM000665.1:g.50339487C>T	GRCh37
NC_000003.10:g.50314491C>T	NCBI36
NG_009295.1:g.15326G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_033159.4:c.900+1G>A MANE Select	NP_149349.2:n.900+1G>A
ENST00000395144.7:c.900+1G>A MANE Select	ENSP00000378576.2:n.900+1G>A
NM_033159.3:c.900+1G>A	NP_149349.2:n.900+1G>A
NM_153281.1:c.900+1G>A	NP_695013.1:n.900+1G>A
NM_153281.2:c.900+1G>A	NP_695013.1:n.900+1G>A
NM_153282.2:c.900+1G>A	NP_695014.1:n.900+1G>A
NM_153282.3:c.900+1G>A	NP_695014.1:n.900+1G>A
NM_153283.2:c.354+1G>A	NP_695015.1:n.354+1G>A
NM_153283.3:c.354+1G>A	NP_695015.1:n.354+1G>A
NM_153285.2:c.123+1G>A	NP_695017.1:n.123+1G>A
NM_153285.3:c.123+1G>A	NP_695017.1:n.123+1G>A
NR_047690.1:n.1545+1G>A
NR_047690.2:n.1518+1G>A
ENST00000266031.8:c.900+1G>A	ENSP00000266031.4:n.900+1G>A
ENST00000320295.12:c.900+1G>A	ENSP00000346068.5:n.900+1G>A
ENST00000395143.6:c.900+1G>A	ENSP00000378575.2:n.900+1G>A
ENST00000395144.6:c.900+1G>A	ENSP00000378576.2:n.900+1G>A
ENST00000447605.2:c.123+1G>A	ENSP00000390149.2:n.123+1G>A
ENST00000457214.6:c.354+1G>A	ENSP00000393358.2:n.354+1G>A
ENST00000618175.4:c.900+1G>A	ENSP00000477903.1:n.900+1G>A
XM_011533667.1:c.900+1G>A	XP_011531969.1:n.900+1G>A
XM_011533667.2:c.900+1G>A	XP_011531969.1:n.900+1G>A
XM_011533668.1:c.900+1G>A	XP_011531970.1:n.900+1G>A
XM_011533668.2:c.900+1G>A	XP_011531970.1:n.900+1G>A
XM_011533669.1:c.900+1G>A	XP_011531971.1:n.900+1G>A
XM_011533669.2:c.900+1G>A	XP_011531971.1:n.900+1G>A