Canonical Allele Identifier: CA455440330

Gene: GUSB

Linked Data

• MyVariant Identifiers: chr7:g.65426028A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.65961041A>G , CM000669.2:g.65961041A>G	GRCh38
NC_000007.13:g.65426028A>G , CM000669.1:g.65426028A>G	GRCh37
NC_000007.12:g.65063463A>G	NCBI36
NG_016197.1:g.26274T>C
NG_051954.1:g.92943A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304895.9:c.1812T>C MANE Select	ENSP00000302728.4:p.Asn604=
ENST00000304895.8:c.1812T>C	ENSP00000302728.4:p.Asn604=
ENST00000421103.5:c.1374T>C	ENSP00000391390.1:p.Asn458=
ENST00000430730.5:c.*1079T>C	ENSP00000411859.1:n.*1079T>C
ENST00000447929.5:c.*1192T>C	ENSP00000411262.1:n.*1192T>C
ENST00000466883.5:n.2202T>C
NM_000181.3:c.1812T>C	NP_000172.2:p.Asn604=
NM_001284290.1:c.1374T>C	NP_001271219.1:p.Asn458=
NM_001293104.1:c.1242T>C	NP_001280033.1:p.Asn414=
NM_001293105.1:c.1155T>C	NP_001280034.1:p.Asn385=
NR_120531.1:n.1858T>C
XM_005250297.3:c.1659T>C	XP_005250354.1:p.Asn553=
XM_011516113.1:c.1311T>C	XP_011514415.1:p.Asn437=
XM_011516114.1:c.1140T>C	XP_011514416.1:p.Asn380=
XM_005250297.4:c.1659T>C	XP_005250354.1:p.Asn553=
XM_011516114.2:c.1140T>C	XP_011514416.1:p.Asn380=
XM_017012091.1:c.1158T>C	XP_016867580.1:p.Asn386=
XM_017012092.1:c.1089T>C	XP_016867581.1:p.Asn363=
XM_017012093.2:c.987T>C	XP_016867582.1:p.Asn329=
XR_001744658.2:n.1619T>C
XR_001744659.2:n.1732T>C
XR_001744660.2:n.1664T>C
XR_001744661.2:n.1579T>C
XR_927461.3:n.1817T>C
NM_000181.4:c.1812T>C MANE Select	NP_000172.2:p.Asn604=
NM_001284290.2:c.1374T>C	NP_001271219.1:p.Asn458=
NM_001293104.2:c.1242T>C	NP_001280033.1:p.Asn414=
NM_001293105.2:c.1155T>C	NP_001280034.1:p.Asn385=
NR_120531.2:n.1757T>C