Canonical Allele Identifier: CA159904403

Gene: GUSB

Linked Data

• dbSNP Id: rs960705802
• gnomAD v3: 7-65960809-G-A
• gnomAD v4: 7-65960809-G-A
• MyVariant Identifiers: chr7:g.65425796G>A (hg19) ; chr7:g.65960809G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.65960809G>A , CM000669.2:g.65960809G>A	GRCh38
NC_000007.13:g.65425796G>A , CM000669.1:g.65425796G>A	GRCh37
NC_000007.12:g.65063231G>A	NCBI36
NG_016197.1:g.26506C>T
NG_051954.1:g.92711G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304895.9:c.*88C>T MANE Select	ENSP00000302728.4:n.*88C>T
ENST00000304895.8:c.*88C>T	ENSP00000302728.4:n.*88C>T
ENST00000421103.5:c.*88C>T	ENSP00000391390.1:n.*88C>T
ENST00000430730.5:c.*1311C>T	ENSP00000411859.1:n.*1311C>T
ENST00000447929.5:c.*1424C>T	ENSP00000411262.1:n.*1424C>T
ENST00000466883.5:n.2434C>T
NM_000181.3:c.*88C>T	NP_000172.2:n.*88C>T
NM_001284290.1:c.*88C>T	NP_001271219.1:n.*88C>T
NM_001293104.1:c.*88C>T	NP_001280033.1:n.*88C>T
NM_001293105.1:c.*88C>T	NP_001280034.1:n.*88C>T
NR_120531.1:n.2090C>T
XM_005250297.3:c.*88C>T	XP_005250354.1:n.*88C>T
XM_011516113.1:c.*88C>T	XP_011514415.1:n.*88C>T
XM_011516114.1:c.*88C>T	XP_011514416.1:n.*88C>T
XM_005250297.4:c.*88C>T	XP_005250354.1:n.*88C>T
XM_011516114.2:c.*88C>T	XP_011514416.1:n.*88C>T
XM_017012091.1:c.*88C>T	XP_016867580.1:n.*88C>T
XM_017012092.1:c.*88C>T	XP_016867581.1:n.*88C>T
XM_017012093.2:c.*88C>T	XP_016867582.1:n.*88C>T
XR_001744658.2:n.1851C>T
XR_001744659.2:n.1964C>T
XR_001744660.2:n.1896C>T
XR_001744661.2:n.1811C>T
XR_927461.3:n.2049C>T
NM_000181.4:c.*88C>T MANE Select	NP_000172.2:n.*88C>T
NM_001284290.2:c.*88C>T	NP_001271219.1:n.*88C>T
NM_001293104.2:c.*88C>T	NP_001280033.1:n.*88C>T
NM_001293105.2:c.*88C>T	NP_001280034.1:n.*88C>T
NR_120531.2:n.1989C>T