Canonical Allele Identifier: CA367636926

Gene: GUSB

Linked Data

• MyVariant Identifiers: chr7:g.65425889T>A (hg19) ; chr7:g.65960902T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.65960902T>A , CM000669.2:g.65960902T>A	GRCh38
NC_000007.13:g.65425889T>A , CM000669.1:g.65425889T>A	GRCh37
NC_000007.12:g.65063324T>A	NCBI36
NG_016197.1:g.26413A>T
NG_051954.1:g.92804T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304895.9:c.1951A>T MANE Select	ENSP00000302728.4:p.Thr651Ser
ENST00000304895.8:c.1951A>T	ENSP00000302728.4:p.Thr651Ser
ENST00000421103.5:c.1513A>T	ENSP00000391390.1:p.Thr505Ser
ENST00000430730.5:c.*1218A>T	ENSP00000411859.1:n.*1218A>T
ENST00000447929.5:c.*1331A>T	ENSP00000411262.1:n.*1331A>T
ENST00000466883.5:n.2341A>T
NM_000181.3:c.1951A>T	NP_000172.2:p.Thr651Ser
NM_001284290.1:c.1513A>T	NP_001271219.1:p.Thr505Ser
NM_001293104.1:c.1381A>T	NP_001280033.1:p.Thr461Ser
NM_001293105.1:c.1294A>T	NP_001280034.1:p.Thr432Ser
NR_120531.1:n.1997A>T
XM_005250297.3:c.1798A>T	XP_005250354.1:p.Thr600Ser
XM_011516113.1:c.1450A>T	XP_011514415.1:p.Thr484Ser
XM_011516114.1:c.1279A>T	XP_011514416.1:p.Thr427Ser
XM_005250297.4:c.1798A>T	XP_005250354.1:p.Thr600Ser
XM_011516114.2:c.1279A>T	XP_011514416.1:p.Thr427Ser
XM_017012091.1:c.1297A>T	XP_016867580.1:p.Thr433Ser
XM_017012092.1:c.1228A>T	XP_016867581.1:p.Thr410Ser
XM_017012093.2:c.1126A>T	XP_016867582.1:p.Thr376Ser
XR_001744658.2:n.1758A>T
XR_001744659.2:n.1871A>T
XR_001744660.2:n.1803A>T
XR_001744661.2:n.1718A>T
XR_927461.3:n.1956A>T
NM_000181.4:c.1951A>T MANE Select	NP_000172.2:p.Thr651Ser
NM_001284290.2:c.1513A>T	NP_001271219.1:p.Thr505Ser
NM_001293104.2:c.1381A>T	NP_001280033.1:p.Thr461Ser
NM_001293105.2:c.1294A>T	NP_001280034.1:p.Thr432Ser
NR_120531.2:n.1896A>T