Canonical Allele Identifier: CA367637621

Gene: GUSB

Linked Data

• MyVariant Identifiers: chr7:g.65426029T>C (hg19) ; chr7:g.65961042T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.65961042T>C , CM000669.2:g.65961042T>C	GRCh38
NC_000007.13:g.65426029T>C , CM000669.1:g.65426029T>C	GRCh37
NC_000007.12:g.65063464T>C	NCBI36
NG_016197.1:g.26273A>G
NG_051954.1:g.92944T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304895.9:c.1811A>G MANE Select	ENSP00000302728.4:p.Asn604Ser
ENST00000304895.8:c.1811A>G	ENSP00000302728.4:p.Asn604Ser
ENST00000421103.5:c.1373A>G	ENSP00000391390.1:p.Asn458Ser
ENST00000430730.5:c.*1078A>G	ENSP00000411859.1:n.*1078A>G
ENST00000447929.5:c.*1191A>G	ENSP00000411262.1:n.*1191A>G
ENST00000466883.5:n.2201A>G
NM_000181.3:c.1811A>G	NP_000172.2:p.Asn604Ser
NM_001284290.1:c.1373A>G	NP_001271219.1:p.Asn458Ser
NM_001293104.1:c.1241A>G	NP_001280033.1:p.Asn414Ser
NM_001293105.1:c.1154A>G	NP_001280034.1:p.Asn385Ser
NR_120531.1:n.1857A>G
XM_005250297.3:c.1658A>G	XP_005250354.1:p.Asn553Ser
XM_011516113.1:c.1310A>G	XP_011514415.1:p.Asn437Ser
XM_011516114.1:c.1139A>G	XP_011514416.1:p.Asn380Ser
XM_005250297.4:c.1658A>G	XP_005250354.1:p.Asn553Ser
XM_011516114.2:c.1139A>G	XP_011514416.1:p.Asn380Ser
XM_017012091.1:c.1157A>G	XP_016867580.1:p.Asn386Ser
XM_017012092.1:c.1088A>G	XP_016867581.1:p.Asn363Ser
XM_017012093.2:c.986A>G	XP_016867582.1:p.Asn329Ser
XR_001744658.2:n.1618A>G
XR_001744659.2:n.1731A>G
XR_001744660.2:n.1663A>G
XR_001744661.2:n.1578A>G
XR_927461.3:n.1816A>G
NM_000181.4:c.1811A>G MANE Select	NP_000172.2:p.Asn604Ser
NM_001284290.2:c.1373A>G	NP_001271219.1:p.Asn458Ser
NM_001293104.2:c.1241A>G	NP_001280033.1:p.Asn414Ser
NM_001293105.2:c.1154A>G	NP_001280034.1:p.Asn385Ser
NR_120531.2:n.1756A>G