Canonical Allele Identifier: CA367637123

Gene: GUSB

Linked Data

• MyVariant Identifiers: chr7:g.65425933G>C (hg19) ; chr7:g.65960946G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.65960946G>C , CM000669.2:g.65960946G>C	GRCh38
NC_000007.13:g.65425933G>C , CM000669.1:g.65425933G>C	GRCh37
NC_000007.12:g.65063368G>C	NCBI36
NG_016197.1:g.26369C>G
NG_051954.1:g.92848G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304895.9:c.1907C>G MANE Select	ENSP00000302728.4:p.Pro636Arg
ENST00000304895.8:c.1907C>G	ENSP00000302728.4:p.Pro636Arg
ENST00000421103.5:c.1469C>G	ENSP00000391390.1:p.Pro490Arg
ENST00000430730.5:c.*1174C>G	ENSP00000411859.1:n.*1174C>G
ENST00000447929.5:c.*1287C>G	ENSP00000411262.1:n.*1287C>G
ENST00000466883.5:n.2297C>G
NM_000181.3:c.1907C>G	NP_000172.2:p.Pro636Arg
NM_001284290.1:c.1469C>G	NP_001271219.1:p.Pro490Arg
NM_001293104.1:c.1337C>G	NP_001280033.1:p.Pro446Arg
NM_001293105.1:c.1250C>G	NP_001280034.1:p.Pro417Arg
NR_120531.1:n.1953C>G
XM_005250297.3:c.1754C>G	XP_005250354.1:p.Pro585Arg
XM_011516113.1:c.1406C>G	XP_011514415.1:p.Pro469Arg
XM_011516114.1:c.1235C>G	XP_011514416.1:p.Pro412Arg
XM_005250297.4:c.1754C>G	XP_005250354.1:p.Pro585Arg
XM_011516114.2:c.1235C>G	XP_011514416.1:p.Pro412Arg
XM_017012091.1:c.1253C>G	XP_016867580.1:p.Pro418Arg
XM_017012092.1:c.1184C>G	XP_016867581.1:p.Pro395Arg
XM_017012093.2:c.1082C>G	XP_016867582.1:p.Pro361Arg
XR_001744658.2:n.1714C>G
XR_001744659.2:n.1827C>G
XR_001744660.2:n.1759C>G
XR_001744661.2:n.1674C>G
XR_927461.3:n.1912C>G
NM_000181.4:c.1907C>G MANE Select	NP_000172.2:p.Pro636Arg
NM_001284290.2:c.1469C>G	NP_001271219.1:p.Pro490Arg
NM_001293104.2:c.1337C>G	NP_001280033.1:p.Pro446Arg
NM_001293105.2:c.1250C>G	NP_001280034.1:p.Pro417Arg
NR_120531.2:n.1852C>G