Canonical Allele Identifier: CA1713890543

Gene: GUSB

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.65982109G= , CM000669.2:g.65982109G=	GRCh38
NC_000007.13:g.65447096G= , CM000669.1:g.65447096G=	GRCh37
NC_000007.12:g.65084531G=	NCBI36
NG_016197.1:g.5206C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000304895.9:c.75C= MANE Select	ENSP00000302728.4:p.Gly25=
ENST00000304895.8:c.75C=	ENSP00000302728.4:p.Gly25=
ENST00000421103.5:c.75C=	ENSP00000391390.1:p.Gly25=
ENST00000430730.5:c.75C=	ENSP00000411859.1:p.Gly25=
ENST00000446111.1:c.75C=	ENSP00000416793.1:p.Gly25=
ENST00000447929.5:c.75C=	ENSP00000411262.1:p.Gly25=
NM_000181.3:c.75C=	NP_000172.2:p.Gly25=
NM_001284290.1:c.75C=	NP_001271219.1:p.Gly25=
NM_001293104.1:c.-311C=	NP_001280033.1:n.-311C=
NM_001293105.1:c.-255C=	NP_001280034.1:n.-255C=
NR_120531.1:n.206C=
XM_005250297.3:c.75C=	XP_005250354.1:p.Gly25=
XM_011516113.1:c.-255C=	XP_011514415.1:n.-255C=
XR_927461.1:n.201C=
XM_005250297.4:c.75C=	XP_005250354.1:p.Gly25=
XM_011516114.2:c.-611C=	XP_011514416.1:n.-611C=
XM_017012091.1:c.-255C=	XP_016867580.1:n.-255C=
XM_017012092.1:c.-311C=	XP_016867581.1:n.-311C=
XM_017012093.2:c.-611C=	XP_016867582.1:n.-611C=
XR_001744658.2:n.120C=
XR_001744659.2:n.120C=
XR_001744660.2:n.120C=
XR_001744661.2:n.120C=
XR_927461.3:n.120C=
NM_000181.4:c.75C= MANE Select	NP_000172.2:p.Gly25=
NM_001284290.2:c.75C=	NP_001271219.1:p.Gly25=
NM_001293104.2:c.-311C=	NP_001280033.1:n.-311C=
NM_001293105.2:c.-255C=	NP_001280034.1:n.-255C=
NR_120531.2:n.105C=