Canonical Allele Identifier: CA367654975

Gene: GUSB

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.65982046G>T , CM000669.2:g.65982046G>T	GRCh38
NC_000007.13:g.65447033G>T , CM000669.1:g.65447033G>T	GRCh37
NC_000007.12:g.65084468G>T	NCBI36
NG_016197.1:g.5269C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304895.9:c.138C>A MANE Select	ENSP00000302728.4:p.Ser46Arg
ENST00000304895.8:c.138C>A	ENSP00000302728.4:p.Ser46Arg
ENST00000421103.5:c.138C>A	ENSP00000391390.1:p.Ser46Arg
ENST00000430730.5:c.138C>A	ENSP00000411859.1:p.Ser46Arg
ENST00000446111.1:c.138C>A	ENSP00000416793.1:p.Ser46Arg
ENST00000447929.5:c.138C>A	ENSP00000411262.1:p.Ser46Arg
ENST00000475316.5:n.43C>A
NM_000181.3:c.138C>A	NP_000172.2:p.Ser46Arg
NM_001284290.1:c.138C>A	NP_001271219.1:p.Ser46Arg
NM_001293104.1:c.-248C>A	NP_001280033.1:n.-248C>A
NM_001293105.1:c.-192C>A	NP_001280034.1:n.-192C>A
NR_120531.1:n.269C>A
XM_005250297.3:c.138C>A	XP_005250354.1:p.Ser46Arg
XM_011516113.1:c.-192C>A	XP_011514415.1:n.-192C>A
XR_927461.1:n.264C>A
XM_005250297.4:c.138C>A	XP_005250354.1:p.Ser46Arg
XM_011516114.2:c.-548C>A	XP_011514416.1:n.-548C>A
XM_017012091.1:c.-192C>A	XP_016867580.1:n.-192C>A
XM_017012092.1:c.-248C>A	XP_016867581.1:n.-248C>A
XM_017012093.2:c.-548C>A	XP_016867582.1:n.-548C>A
XR_001744658.2:n.183C>A
XR_001744659.2:n.183C>A
XR_001744660.2:n.183C>A
XR_001744661.2:n.183C>A
XR_927461.3:n.183C>A
NM_000181.4:c.138C>A MANE Select	NP_000172.2:p.Ser46Arg
NM_001284290.2:c.138C>A	NP_001271219.1:p.Ser46Arg
NM_001293104.2:c.-248C>A	NP_001280033.1:n.-248C>A
NM_001293105.2:c.-192C>A	NP_001280034.1:n.-192C>A
NR_120531.2:n.168C>A