Canonical Allele Identifier: CA2683077415

Gene: GUSB

Linked Data

• gnomAD v4: 7-65960799-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.65960800del , CM000669.2:g.65960800del	GRCh38
NC_000007.13:g.65425787del , CM000669.1:g.65425787del	GRCh37
NC_000007.12:g.65063222del	NCBI36
NG_016197.1:g.26515del
NG_051954.1:g.92702del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304895.9:c.*97del MANE Select	ENSP00000302728.4:n.*97del
ENST00000304895.8:c.*97del	ENSP00000302728.4:n.*97del
ENST00000421103.5:c.*97del	ENSP00000391390.1:n.*97del
ENST00000430730.5:c.*1320del	ENSP00000411859.1:n.*1320del
ENST00000447929.5:c.*1433del	ENSP00000411262.1:n.*1433del
ENST00000466883.5:n.2443del
NM_000181.3:c.*97del	NP_000172.2:n.*97del
NM_001284290.1:c.*97del	NP_001271219.1:n.*97del
NM_001293104.1:c.*97del	NP_001280033.1:n.*97del
NM_001293105.1:c.*97del	NP_001280034.1:n.*97del
NR_120531.1:n.2099del
XM_005250297.3:c.*97del	XP_005250354.1:n.*97del
XM_011516113.1:c.*97del	XP_011514415.1:n.*97del
XM_011516114.1:c.*97del	XP_011514416.1:n.*97del
XM_005250297.4:c.*97del	XP_005250354.1:n.*97del
XM_011516114.2:c.*97del	XP_011514416.1:n.*97del
XM_017012091.1:c.*97del	XP_016867580.1:n.*97del
XM_017012092.1:c.*97del	XP_016867581.1:n.*97del
XM_017012093.2:c.*97del	XP_016867582.1:n.*97del
XR_001744658.2:n.1860del
XR_001744659.2:n.1973del
XR_001744660.2:n.1905del
XR_001744661.2:n.1820del
XR_927461.3:n.2058del
NM_000181.4:c.*97del MANE Select	NP_000172.2:n.*97del
NM_001284290.2:c.*97del	NP_001271219.1:n.*97del
NM_001293104.2:c.*97del	NP_001280033.1:n.*97del
NM_001293105.2:c.*97del	NP_001280034.1:n.*97del
NR_120531.2:n.1998del