Canonical Allele Identifier: CA367637335

Gene: GUSB

Linked Data

• MyVariant Identifiers: chr7:g.65425981A>C (hg19) ; chr7:g.65960994A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.65960994A>C , CM000669.2:g.65960994A>C	GRCh38
NC_000007.13:g.65425981A>C , CM000669.1:g.65425981A>C	GRCh37
NC_000007.12:g.65063416A>C	NCBI36
NG_016197.1:g.26321T>G
NG_051954.1:g.92896A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304895.9:c.1859T>G MANE Select	ENSP00000302728.4:p.Phe620Cys
ENST00000304895.8:c.1859T>G	ENSP00000302728.4:p.Phe620Cys
ENST00000421103.5:c.1421T>G	ENSP00000391390.1:p.Phe474Cys
ENST00000430730.5:c.*1126T>G	ENSP00000411859.1:n.*1126T>G
ENST00000447929.5:c.*1239T>G	ENSP00000411262.1:n.*1239T>G
ENST00000466883.5:n.2249T>G
NM_000181.3:c.1859T>G	NP_000172.2:p.Phe620Cys
NM_001284290.1:c.1421T>G	NP_001271219.1:p.Phe474Cys
NM_001293104.1:c.1289T>G	NP_001280033.1:p.Phe430Cys
NM_001293105.1:c.1202T>G	NP_001280034.1:p.Phe401Cys
NR_120531.1:n.1905T>G
XM_005250297.3:c.1706T>G	XP_005250354.1:p.Phe569Cys
XM_011516113.1:c.1358T>G	XP_011514415.1:p.Phe453Cys
XM_011516114.1:c.1187T>G	XP_011514416.1:p.Phe396Cys
XM_005250297.4:c.1706T>G	XP_005250354.1:p.Phe569Cys
XM_011516114.2:c.1187T>G	XP_011514416.1:p.Phe396Cys
XM_017012091.1:c.1205T>G	XP_016867580.1:p.Phe402Cys
XM_017012092.1:c.1136T>G	XP_016867581.1:p.Phe379Cys
XM_017012093.2:c.1034T>G	XP_016867582.1:p.Phe345Cys
XR_001744658.2:n.1666T>G
XR_001744659.2:n.1779T>G
XR_001744660.2:n.1711T>G
XR_001744661.2:n.1626T>G
XR_927461.3:n.1864T>G
NM_000181.4:c.1859T>G MANE Select	NP_000172.2:p.Phe620Cys
NM_001284290.2:c.1421T>G	NP_001271219.1:p.Phe474Cys
NM_001293104.2:c.1289T>G	NP_001280033.1:p.Phe430Cys
NM_001293105.2:c.1202T>G	NP_001280034.1:p.Phe401Cys
NR_120531.2:n.1804T>G