Canonical Allele Identifier: CA1713854267

Gene: GUSB

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.65960856G= , CM000669.2:g.65960856G=	GRCh38
NC_000007.13:g.65425843G= , CM000669.1:g.65425843G=	GRCh37
NC_000007.12:g.65063278G=	NCBI36
NG_016197.1:g.26459C=
NG_051954.1:g.92758G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304895.9:c.*41C= MANE Select	ENSP00000302728.4:n.*41C=
ENST00000304895.8:c.*41C=	ENSP00000302728.4:n.*41C=
ENST00000421103.5:c.*41C=	ENSP00000391390.1:n.*41C=
ENST00000430730.5:c.*1264C=	ENSP00000411859.1:n.*1264C=
ENST00000447929.5:c.*1377C=	ENSP00000411262.1:n.*1377C=
ENST00000466883.5:n.2387C=
NM_000181.3:c.*41C=	NP_000172.2:n.*41C=
NM_001284290.1:c.*41C=	NP_001271219.1:n.*41C=
NM_001293104.1:c.*41C=	NP_001280033.1:n.*41C=
NM_001293105.1:c.*41C=	NP_001280034.1:n.*41C=
NR_120531.1:n.2043C=
XM_005250297.3:c.*41C=	XP_005250354.1:n.*41C=
XM_011516113.1:c.*41C=	XP_011514415.1:n.*41C=
XM_011516114.1:c.*41C=	XP_011514416.1:n.*41C=
XM_005250297.4:c.*41C=	XP_005250354.1:n.*41C=
XM_011516114.2:c.*41C=	XP_011514416.1:n.*41C=
XM_017012091.1:c.*41C=	XP_016867580.1:n.*41C=
XM_017012092.1:c.*41C=	XP_016867581.1:n.*41C=
XM_017012093.2:c.*41C=	XP_016867582.1:n.*41C=
XR_001744658.2:n.1804C=
XR_001744659.2:n.1917C=
XR_001744660.2:n.1849C=
XR_001744661.2:n.1764C=
XR_927461.3:n.2002C=
NM_000181.4:c.*41C= MANE Select	NP_000172.2:n.*41C=
NM_001284290.2:c.*41C=	NP_001271219.1:n.*41C=
NM_001293104.2:c.*41C=	NP_001280033.1:n.*41C=
NM_001293105.2:c.*41C=	NP_001280034.1:n.*41C=
NR_120531.2:n.1942C=