Canonical Allele Identifier: CA1713854612

Gene: GUSB

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.65960966A= , CM000669.2:g.65960966A=	GRCh38
NC_000007.13:g.65425953A= , CM000669.1:g.65425953A=	GRCh37
NC_000007.12:g.65063388A=	NCBI36
NG_016197.1:g.26349T=
NG_051954.1:g.92868A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304895.9:c.1887T= MANE Select	ENSP00000302728.4:p.Ile629=
ENST00000304895.8:c.1887T=	ENSP00000302728.4:p.Ile629=
ENST00000421103.5:c.1449T=	ENSP00000391390.1:p.Ile483=
ENST00000430730.5:c.*1154T=	ENSP00000411859.1:n.*1154T=
ENST00000447929.5:c.*1267T=	ENSP00000411262.1:n.*1267T=
ENST00000466883.5:n.2277T=
NM_000181.3:c.1887T=	NP_000172.2:p.Ile629=
NM_001284290.1:c.1449T=	NP_001271219.1:p.Ile483=
NM_001293104.1:c.1317T=	NP_001280033.1:p.Ile439=
NM_001293105.1:c.1230T=	NP_001280034.1:p.Ile410=
NR_120531.1:n.1933T=
XM_005250297.3:c.1734T=	XP_005250354.1:p.Ile578=
XM_011516113.1:c.1386T=	XP_011514415.1:p.Ile462=
XM_011516114.1:c.1215T=	XP_011514416.1:p.Ile405=
XM_005250297.4:c.1734T=	XP_005250354.1:p.Ile578=
XM_011516114.2:c.1215T=	XP_011514416.1:p.Ile405=
XM_017012091.1:c.1233T=	XP_016867580.1:p.Ile411=
XM_017012092.1:c.1164T=	XP_016867581.1:p.Ile388=
XM_017012093.2:c.1062T=	XP_016867582.1:p.Ile354=
XR_001744658.2:n.1694T=
XR_001744659.2:n.1807T=
XR_001744660.2:n.1739T=
XR_001744661.2:n.1654T=
XR_927461.3:n.1892T=
NM_000181.4:c.1887T= MANE Select	NP_000172.2:p.Ile629=
NM_001284290.2:c.1449T=	NP_001271219.1:p.Ile483=
NM_001293104.2:c.1317T=	NP_001280033.1:p.Ile439=
NM_001293105.2:c.1230T=	NP_001280034.1:p.Ile410=
NR_120531.2:n.1832T=