Canonical Allele Identifier: CA1713864991

Gene: GUSB

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.65967912G= , CM000669.2:g.65967912G=	GRCh38
NC_000007.13:g.65432899G= , CM000669.1:g.65432899G=	GRCh37
NC_000007.12:g.65070334G=	NCBI36
NG_016197.1:g.19403C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000304895.9:c.1477-5C= MANE Select	ENSP00000302728.4:n.1477-5C=
ENST00000304895.8:c.1477-5C=	ENSP00000302728.4:n.1477-5C=
ENST00000421103.5:c.1039-5C=	ENSP00000391390.1:n.1039-5C=
ENST00000430730.5:c.*744-5C=	ENSP00000411859.1:n.*744-5C=
ENST00000447929.5:c.*857-5C=	ENSP00000411262.1:n.*857-5C=
ENST00000462371.1:n.515-5C=
ENST00000466883.5:n.1867-5C=
NM_000181.3:c.1477-5C=	NP_000172.2:n.1477-5C=
NM_001284290.1:c.1039-5C=	NP_001271219.1:n.1039-5C=
NM_001293104.1:c.907-5C=	NP_001280033.1:n.907-5C=
NM_001293105.1:c.820-5C=	NP_001280034.1:n.820-5C=
NR_120531.1:n.1523-5C=
XM_005250297.3:c.1324-5C=	XP_005250354.1:n.1324-5C=
XM_011516113.1:c.976-5C=	XP_011514415.1:n.976-5C=
XM_011516114.1:c.805-5C=	XP_011514416.1:n.805-5C=
XR_927461.1:n.1563-5C=
XM_005250297.4:c.1324-5C=	XP_005250354.1:n.1324-5C=
XM_011516114.2:c.805-5C=	XP_011514416.1:n.805-5C=
XM_017012091.1:c.823-5C=	XP_016867580.1:n.823-5C=
XM_017012092.1:c.754-5C=	XP_016867581.1:n.754-5C=
XM_017012093.2:c.652-5C=	XP_016867582.1:n.652-5C=
XR_001744658.2:n.1284-5C=
XR_001744659.2:n.1397-5C=
XR_001744660.2:n.1329-5C=
XR_001744661.2:n.1244-5C=
XR_927461.3:n.1482-5C=
NM_000181.4:c.1477-5C= MANE Select	NP_000172.2:n.1477-5C=
NM_001284290.2:c.1039-5C=	NP_001271219.1:n.1039-5C=
NM_001293104.2:c.907-5C=	NP_001280033.1:n.907-5C=
NM_001293105.2:c.820-5C=	NP_001280034.1:n.820-5C=
NR_120531.2:n.1422-5C=