Canonical Allele Identifier: CA455449311

Gene: GUSB

Linked Data

• MyVariant Identifiers: chr7:g.65447024G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.65982037G>T , CM000669.2:g.65982037G>T	GRCh38
NC_000007.13:g.65447024G>T , CM000669.1:g.65447024G>T	GRCh37
NC_000007.12:g.65084459G>T	NCBI36
NG_016197.1:g.5278C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304895.9:c.147C>A MANE Select	ENSP00000302728.4:p.Ala49=
ENST00000304895.8:c.147C>A	ENSP00000302728.4:p.Ala49=
ENST00000421103.5:c.147C>A	ENSP00000391390.1:p.Ala49=
ENST00000430730.5:c.147C>A	ENSP00000411859.1:p.Ala49=
ENST00000446111.1:c.147C>A	ENSP00000416793.1:p.Ala49=
ENST00000447929.5:c.147C>A	ENSP00000411262.1:p.Ala49=
ENST00000475316.5:n.52C>A
NM_000181.3:c.147C>A	NP_000172.2:p.Ala49=
NM_001284290.1:c.147C>A	NP_001271219.1:p.Ala49=
NM_001293104.1:c.-239C>A	NP_001280033.1:n.-239C>A
NM_001293105.1:c.-183C>A	NP_001280034.1:n.-183C>A
NR_120531.1:n.278C>A
XM_005250297.3:c.147C>A	XP_005250354.1:p.Ala49=
XM_011516113.1:c.-183C>A	XP_011514415.1:n.-183C>A
XR_927461.1:n.273C>A
XM_005250297.4:c.147C>A	XP_005250354.1:p.Ala49=
XM_011516114.2:c.-539C>A	XP_011514416.1:n.-539C>A
XM_017012091.1:c.-183C>A	XP_016867580.1:n.-183C>A
XM_017012092.1:c.-239C>A	XP_016867581.1:n.-239C>A
XM_017012093.2:c.-539C>A	XP_016867582.1:n.-539C>A
XR_001744658.2:n.192C>A
XR_001744659.2:n.192C>A
XR_001744660.2:n.192C>A
XR_001744661.2:n.192C>A
XR_927461.3:n.192C>A
NM_000181.4:c.147C>A MANE Select	NP_000172.2:p.Ala49=
NM_001284290.2:c.147C>A	NP_001271219.1:p.Ala49=
NM_001293104.2:c.-239C>A	NP_001280033.1:n.-239C>A
NM_001293105.2:c.-183C>A	NP_001280034.1:n.-183C>A
NR_120531.2:n.177C>A