Canonical Allele Identifier: CA367655718

Gene: GUSB

Linked Data

• gnomAD v4: 7-65982159-A-T
• MyVariant Identifiers: chr7:g.65447146A>T (hg19) ; chr7:g.65982159A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.65982159A>T , CM000669.2:g.65982159A>T	GRCh38
NC_000007.13:g.65447146A>T , CM000669.1:g.65447146A>T	GRCh37
NC_000007.12:g.65084581A>T	NCBI36
NG_016197.1:g.5156T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304895.9:c.25T>A MANE Select	ENSP00000302728.4:p.Trp9Arg
ENST00000304895.8:c.25T>A	ENSP00000302728.4:p.Trp9Arg
ENST00000421103.5:c.25T>A	ENSP00000391390.1:p.Trp9Arg
ENST00000430730.5:c.25T>A	ENSP00000411859.1:p.Trp9Arg
ENST00000446111.1:c.25T>A	ENSP00000416793.1:p.Trp9Arg
ENST00000447929.5:c.25T>A	ENSP00000411262.1:p.Trp9Arg
NM_000181.3:c.25T>A	NP_000172.2:p.Trp9Arg
NM_001284290.1:c.25T>A	NP_001271219.1:p.Trp9Arg
NM_001293104.1:c.-361T>A	NP_001280033.1:n.-361T>A
NM_001293105.1:c.-305T>A	NP_001280034.1:n.-305T>A
NR_120531.1:n.156T>A
XM_005250297.3:c.25T>A	XP_005250354.1:p.Trp9Arg
XM_011516113.1:c.-305T>A	XP_011514415.1:n.-305T>A
XR_927461.1:n.151T>A
XM_005250297.4:c.25T>A	XP_005250354.1:p.Trp9Arg
XM_011516114.2:c.-661T>A	XP_011514416.1:n.-661T>A
XM_017012091.1:c.-305T>A	XP_016867580.1:n.-305T>A
XM_017012092.1:c.-361T>A	XP_016867581.1:n.-361T>A
XM_017012093.2:c.-661T>A	XP_016867582.1:n.-661T>A
XR_001744658.2:n.70T>A
XR_001744659.2:n.70T>A
XR_001744660.2:n.70T>A
XR_001744661.2:n.70T>A
XR_927461.3:n.70T>A
NM_000181.4:c.25T>A MANE Select	NP_000172.2:p.Trp9Arg
NM_001284290.2:c.25T>A	NP_001271219.1:p.Trp9Arg
NM_001293104.2:c.-361T>A	NP_001280033.1:n.-361T>A
NM_001293105.2:c.-305T>A	NP_001280034.1:n.-305T>A
NR_120531.2:n.55T>A