Canonical Allele Identifier: CA367655460
Gene: GUSB HGNC NCBI

Linked Data

gnomAD v4: 7-65982114-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.65982114G>T , CM000669.2:g.65982114G>T GRCh38
NC_000007.13:g.65447101G>T , CM000669.1:g.65447101G>T GRCh37
NC_000007.12:g.65084536G>T NCBI36
NG_016197.1:g.5201C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000304895.9:c.70C>A MANE Select ENSP00000302728.4:p.Gln24Lys
ENST00000304895.8:c.70C>A ENSP00000302728.4:p.Gln24Lys
ENST00000421103.5:c.70C>A ENSP00000391390.1:p.Gln24Lys
ENST00000430730.5:c.70C>A ENSP00000411859.1:p.Gln24Lys
ENST00000446111.1:c.70C>A ENSP00000416793.1:p.Gln24Lys
ENST00000447929.5:c.70C>A ENSP00000411262.1:p.Gln24Lys
NM_000181.3:c.70C>A NP_000172.2:p.Gln24Lys
NM_001284290.1:c.70C>A NP_001271219.1:p.Gln24Lys
NM_001293104.1:c.-316C>A NP_001280033.1:n.-316C>A
NM_001293105.1:c.-260C>A NP_001280034.1:n.-260C>A
NR_120531.1:n.201C>A
XM_005250297.3:c.70C>A XP_005250354.1:p.Gln24Lys
XM_011516113.1:c.-260C>A XP_011514415.1:n.-260C>A
XR_927461.1:n.196C>A
XM_005250297.4:c.70C>A XP_005250354.1:p.Gln24Lys
XM_011516114.2:c.-616C>A XP_011514416.1:n.-616C>A
XM_017012091.1:c.-260C>A XP_016867580.1:n.-260C>A
XM_017012092.1:c.-316C>A XP_016867581.1:n.-316C>A
XM_017012093.2:c.-616C>A XP_016867582.1:n.-616C>A
XR_001744658.2:n.115C>A
XR_001744659.2:n.115C>A
XR_001744660.2:n.115C>A
XR_001744661.2:n.115C>A
XR_927461.3:n.115C>A
NM_000181.4:c.70C>A MANE Select NP_000172.2:p.Gln24Lys
NM_001284290.2:c.70C>A NP_001271219.1:p.Gln24Lys
NM_001293104.2:c.-316C>A NP_001280033.1:n.-316C>A
NM_001293105.2:c.-260C>A NP_001280034.1:n.-260C>A
NR_120531.2:n.100C>A