Canonical Allele Identifier: CA367637129

Gene: GUSB

Linked Data

• MyVariant Identifiers: chr7:g.65425934G>T (hg19) ; chr7:g.65960947G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.65960947G>T , CM000669.2:g.65960947G>T	GRCh38
NC_000007.13:g.65425934G>T , CM000669.1:g.65425934G>T	GRCh37
NC_000007.12:g.65063369G>T	NCBI36
NG_016197.1:g.26368C>A
NG_051954.1:g.92849G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304895.9:c.1906C>A MANE Select	ENSP00000302728.4:p.Pro636Thr
ENST00000304895.8:c.1906C>A	ENSP00000302728.4:p.Pro636Thr
ENST00000421103.5:c.1468C>A	ENSP00000391390.1:p.Pro490Thr
ENST00000430730.5:c.*1173C>A	ENSP00000411859.1:n.*1173C>A
ENST00000447929.5:c.*1286C>A	ENSP00000411262.1:n.*1286C>A
ENST00000466883.5:n.2296C>A
NM_000181.3:c.1906C>A	NP_000172.2:p.Pro636Thr
NM_001284290.1:c.1468C>A	NP_001271219.1:p.Pro490Thr
NM_001293104.1:c.1336C>A	NP_001280033.1:p.Pro446Thr
NM_001293105.1:c.1249C>A	NP_001280034.1:p.Pro417Thr
NR_120531.1:n.1952C>A
XM_005250297.3:c.1753C>A	XP_005250354.1:p.Pro585Thr
XM_011516113.1:c.1405C>A	XP_011514415.1:p.Pro469Thr
XM_011516114.1:c.1234C>A	XP_011514416.1:p.Pro412Thr
XM_005250297.4:c.1753C>A	XP_005250354.1:p.Pro585Thr
XM_011516114.2:c.1234C>A	XP_011514416.1:p.Pro412Thr
XM_017012091.1:c.1252C>A	XP_016867580.1:p.Pro418Thr
XM_017012092.1:c.1183C>A	XP_016867581.1:p.Pro395Thr
XM_017012093.2:c.1081C>A	XP_016867582.1:p.Pro361Thr
XR_001744658.2:n.1713C>A
XR_001744659.2:n.1826C>A
XR_001744660.2:n.1758C>A
XR_001744661.2:n.1673C>A
XR_927461.3:n.1911C>A
NM_000181.4:c.1906C>A MANE Select	NP_000172.2:p.Pro636Thr
NM_001284290.2:c.1468C>A	NP_001271219.1:p.Pro490Thr
NM_001293104.2:c.1336C>A	NP_001280033.1:p.Pro446Thr
NM_001293105.2:c.1249C>A	NP_001280034.1:p.Pro417Thr
NR_120531.2:n.1851C>A