Canonical Allele Identifier: CA367654967

Gene: GUSB

Linked Data

• gnomAD v4: 7-65982045-A-C
• MyVariant Identifiers: chr7:g.65447032A>C (hg19) ; chr7:g.65982045A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.65982045A>C , CM000669.2:g.65982045A>C	GRCh38
NC_000007.13:g.65447032A>C , CM000669.1:g.65447032A>C	GRCh37
NC_000007.12:g.65084467A>C	NCBI36
NG_016197.1:g.5270T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000304895.9:c.139T>G MANE Select	ENSP00000302728.4:p.Phe47Val
ENST00000304895.8:c.139T>G	ENSP00000302728.4:p.Phe47Val
ENST00000421103.5:c.139T>G	ENSP00000391390.1:p.Phe47Val
ENST00000430730.5:c.139T>G	ENSP00000411859.1:p.Phe47Val
ENST00000446111.1:c.139T>G	ENSP00000416793.1:p.Phe47Val
ENST00000447929.5:c.139T>G	ENSP00000411262.1:p.Phe47Val
ENST00000475316.5:n.44T>G
NM_000181.3:c.139T>G	NP_000172.2:p.Phe47Val
NM_001284290.1:c.139T>G	NP_001271219.1:p.Phe47Val
NM_001293104.1:c.-247T>G	NP_001280033.1:n.-247T>G
NM_001293105.1:c.-191T>G	NP_001280034.1:n.-191T>G
NR_120531.1:n.270T>G
XM_005250297.3:c.139T>G	XP_005250354.1:p.Phe47Val
XM_011516113.1:c.-191T>G	XP_011514415.1:n.-191T>G
XR_927461.1:n.265T>G
XM_005250297.4:c.139T>G	XP_005250354.1:p.Phe47Val
XM_011516114.2:c.-547T>G	XP_011514416.1:n.-547T>G
XM_017012091.1:c.-191T>G	XP_016867580.1:n.-191T>G
XM_017012092.1:c.-247T>G	XP_016867581.1:n.-247T>G
XM_017012093.2:c.-547T>G	XP_016867582.1:n.-547T>G
XR_001744658.2:n.184T>G
XR_001744659.2:n.184T>G
XR_001744660.2:n.184T>G
XR_001744661.2:n.184T>G
XR_927461.3:n.184T>G
NM_000181.4:c.139T>G MANE Select	NP_000172.2:p.Phe47Val
NM_001284290.2:c.139T>G	NP_001271219.1:p.Phe47Val
NM_001293104.2:c.-247T>G	NP_001280033.1:n.-247T>G
NM_001293105.2:c.-191T>G	NP_001280034.1:n.-191T>G
NR_120531.2:n.169T>G