Canonical Allele Identifier: CA2683078606

Gene: GUSB

Linked Data

• gnomAD v4: 7-65967915-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.65967915C>G , CM000669.2:g.65967915C>G	GRCh38
NC_000007.13:g.65432902C>G , CM000669.1:g.65432902C>G	GRCh37
NC_000007.12:g.65070337C>G	NCBI36
NG_016197.1:g.19400G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000304895.9:c.1477-8G>C MANE Select	ENSP00000302728.4:n.1477-8G>C
ENST00000304895.8:c.1477-8G>C	ENSP00000302728.4:n.1477-8G>C
ENST00000421103.5:c.1039-8G>C	ENSP00000391390.1:n.1039-8G>C
ENST00000430730.5:c.*744-8G>C	ENSP00000411859.1:n.*744-8G>C
ENST00000447929.5:c.*857-8G>C	ENSP00000411262.1:n.*857-8G>C
ENST00000462371.1:n.515-8G>C
ENST00000466883.5:n.1867-8G>C
NM_000181.3:c.1477-8G>C	NP_000172.2:n.1477-8G>C
NM_001284290.1:c.1039-8G>C	NP_001271219.1:n.1039-8G>C
NM_001293104.1:c.907-8G>C	NP_001280033.1:n.907-8G>C
NM_001293105.1:c.820-8G>C	NP_001280034.1:n.820-8G>C
NR_120531.1:n.1523-8G>C
XM_005250297.3:c.1324-8G>C	XP_005250354.1:n.1324-8G>C
XM_011516113.1:c.976-8G>C	XP_011514415.1:n.976-8G>C
XM_011516114.1:c.805-8G>C	XP_011514416.1:n.805-8G>C
XR_927461.1:n.1563-8G>C
XM_005250297.4:c.1324-8G>C	XP_005250354.1:n.1324-8G>C
XM_011516114.2:c.805-8G>C	XP_011514416.1:n.805-8G>C
XM_017012091.1:c.823-8G>C	XP_016867580.1:n.823-8G>C
XM_017012092.1:c.754-8G>C	XP_016867581.1:n.754-8G>C
XM_017012093.2:c.652-8G>C	XP_016867582.1:n.652-8G>C
XR_001744658.2:n.1284-8G>C
XR_001744659.2:n.1397-8G>C
XR_001744660.2:n.1329-8G>C
XR_001744661.2:n.1244-8G>C
XR_927461.3:n.1482-8G>C
NM_000181.4:c.1477-8G>C MANE Select	NP_000172.2:n.1477-8G>C
NM_001284290.2:c.1039-8G>C	NP_001271219.1:n.1039-8G>C
NM_001293104.2:c.907-8G>C	NP_001280033.1:n.907-8G>C
NM_001293105.2:c.820-8G>C	NP_001280034.1:n.820-8G>C
NR_120531.2:n.1422-8G>C