Canonical Allele Identifier: CA2683078596

Gene: GUSB

Linked Data

• gnomAD v4: 7-65974277-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.65974277C>T , CM000669.2:g.65974277C>T	GRCh38
NC_000007.13:g.65439264C>T , CM000669.1:g.65439264C>T	GRCh37
NC_000007.12:g.65076699C>T	NCBI36
NG_016197.1:g.13038G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000304895.9:c.1391+18G>A MANE Select	ENSP00000302728.4:n.1391+18G>A
ENST00000304895.8:c.1391+18G>A	ENSP00000302728.4:n.1391+18G>A
ENST00000421103.5:c.953+18G>A	ENSP00000391390.1:n.953+18G>A
ENST00000430730.5:c.*658+18G>A	ENSP00000411859.1:n.*658+18G>A
ENST00000447929.5:c.*771+18G>A	ENSP00000411262.1:n.*771+18G>A
ENST00000462371.1:n.429+18G>A
ENST00000466883.5:n.1866+18G>A
NM_000181.3:c.1391+18G>A	NP_000172.2:n.1391+18G>A
NM_001284290.1:c.953+18G>A	NP_001271219.1:n.953+18G>A
NM_001293104.1:c.821+18G>A	NP_001280033.1:n.821+18G>A
NM_001293105.1:c.734+18G>A	NP_001280034.1:n.734+18G>A
NR_120531.1:n.1522+18G>A
XM_005250297.3:c.1238+18G>A	XP_005250354.1:n.1238+18G>A
XM_011516113.1:c.890+18G>A	XP_011514415.1:n.890+18G>A
XM_011516114.1:c.719+18G>A	XP_011514416.1:n.719+18G>A
XR_927461.1:n.1477+18G>A
XM_005250297.4:c.1238+18G>A	XP_005250354.1:n.1238+18G>A
XM_011516114.2:c.719+18G>A	XP_011514416.1:n.719+18G>A
XM_017012091.1:c.737+18G>A	XP_016867580.1:n.737+18G>A
XM_017012092.1:c.668+18G>A	XP_016867581.1:n.668+18G>A
XM_017012093.2:c.566+18G>A	XP_016867582.1:n.566+18G>A
XR_001744658.2:n.1283+18G>A
XR_001744659.2:n.1396+18G>A
XR_001744660.2:n.1243+18G>A
XR_001744661.2:n.1243+18G>A
XR_927461.3:n.1396+18G>A
NM_000181.4:c.1391+18G>A MANE Select	NP_000172.2:n.1391+18G>A
NM_001284290.2:c.953+18G>A	NP_001271219.1:n.953+18G>A
NM_001293104.2:c.821+18G>A	NP_001280033.1:n.821+18G>A
NM_001293105.2:c.734+18G>A	NP_001280034.1:n.734+18G>A
NR_120531.2:n.1421+18G>A