Canonical Allele Identifier: CA2683078487

Gene: GUSB

Linked Data

• gnomAD v4: 7-65967715-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.65967715G>T , CM000669.2:g.65967715G>T	GRCh38
NC_000007.13:g.65432702G>T , CM000669.1:g.65432702G>T	GRCh37
NC_000007.12:g.65070137G>T	NCBI36
NG_016197.1:g.19600C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304895.9:c.1653+16C>A MANE Select	ENSP00000302728.4:n.1653+16C>A
ENST00000304895.8:c.1653+16C>A	ENSP00000302728.4:n.1653+16C>A
ENST00000421103.5:c.1215+16C>A	ENSP00000391390.1:n.1215+16C>A
ENST00000430730.5:c.*920+16C>A	ENSP00000411859.1:n.*920+16C>A
ENST00000447929.5:c.*1033+16C>A	ENSP00000411262.1:n.*1033+16C>A
ENST00000461622.1:n.178+16C>A
ENST00000462371.1:n.691+16C>A
ENST00000466883.5:n.2043+16C>A
NM_000181.3:c.1653+16C>A	NP_000172.2:n.1653+16C>A
NM_001284290.1:c.1215+16C>A	NP_001271219.1:n.1215+16C>A
NM_001293104.1:c.1083+16C>A	NP_001280033.1:n.1083+16C>A
NM_001293105.1:c.996+16C>A	NP_001280034.1:n.996+16C>A
NR_120531.1:n.1699+16C>A
XM_005250297.3:c.1500+16C>A	XP_005250354.1:n.1500+16C>A
XM_011516113.1:c.1152+16C>A	XP_011514415.1:n.1152+16C>A
XM_011516114.1:c.981+16C>A	XP_011514416.1:n.981+16C>A
XR_927461.1:n.1739+16C>A
XM_005250297.4:c.1500+16C>A	XP_005250354.1:n.1500+16C>A
XM_011516114.2:c.981+16C>A	XP_011514416.1:n.981+16C>A
XM_017012091.1:c.999+16C>A	XP_016867580.1:n.999+16C>A
XM_017012092.1:c.930+16C>A	XP_016867581.1:n.930+16C>A
XM_017012093.2:c.828+16C>A	XP_016867582.1:n.828+16C>A
XR_001744658.2:n.1460+16C>A
XR_001744659.2:n.1573+16C>A
XR_001744660.2:n.1505+16C>A
XR_001744661.2:n.1420+16C>A
XR_927461.3:n.1658+16C>A
NM_000181.4:c.1653+16C>A MANE Select	NP_000172.2:n.1653+16C>A
NM_001284290.2:c.1215+16C>A	NP_001271219.1:n.1215+16C>A
NM_001293104.2:c.1083+16C>A	NP_001280033.1:n.1083+16C>A
NM_001293105.2:c.996+16C>A	NP_001280034.1:n.996+16C>A
NR_120531.2:n.1598+16C>A