Canonical Allele Identifier: CA14863463
Gene: UBASH3A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.42421718G>A , CM000683.2:g.42421718G>A GRCh38
NC_000021.8:g.43841827G>A , CM000683.1:g.43841827G>A GRCh37
NC_000021.7:g.42714896G>A NCBI36
NG_029750.1:g.22857G>A
NG_029750.2:g.22857G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000319294.11:c.1046+3109G>A MANE Select ENSP00000317327.6:n.1046+3109G>A
ENST00000291535.11:c.932+3109G>A ENSP00000291535.6:n.932+3109G>A
ENST00000319294.10:c.1046+3109G>A ENSP00000317327.6:n.1046+3109G>A
ENST00000398367.1:c.932+3109G>A ENSP00000381408.1:n.932+3109G>A
ENST00000473381.1:c.932+3109G>A ENSP00000489235.1:n.932+3109G>A
ENST00000635325.1:c.932+3109G>A ENSP00000489463.1:n.932+3109G>A
NM_001001895.2:c.932+3109G>A NP_001001895.1:n.932+3109G>A
NM_001243467.1:c.932+3109G>A NP_001230396.1:n.932+3109G>A
NM_018961.3:c.1046+3109G>A NP_061834.1:n.1046+3109G>A
XM_006724013.2:c.989+3109G>A XP_006724076.1:n.989+3109G>A
XM_011529605.1:c.1046+3109G>A XP_011527907.1:n.1046+3109G>A
XM_011529606.1:c.641+3109G>A XP_011527908.1:n.641+3109G>A
XM_011529607.1:c.641+3109G>A XP_011527909.1:n.641+3109G>A
XM_011529608.1:c.1046+3109G>A XP_011527910.1:n.1046+3109G>A
XM_011529609.1:c.1046+3109G>A XP_011527911.1:n.1046+3109G>A
XM_011529610.1:c.230+3109G>A XP_011527912.1:n.230+3109G>A
XR_244316.1:n.1016+3109G>A
XR_937510.1:n.1016+3109G>A
XM_006724013.3:c.989+3109G>A XP_006724076.1:n.989+3109G>A
XM_011529605.3:c.1046+3109G>A XP_011527907.1:n.1046+3109G>A
XM_011529606.3:c.641+3109G>A XP_011527908.1:n.641+3109G>A
XM_011529607.2:c.641+3109G>A XP_011527909.1:n.641+3109G>A
XM_011529609.2:c.1046+3109G>A XP_011527911.1:n.1046+3109G>A
XM_011529610.2:c.230+3109G>A XP_011527912.1:n.230+3109G>A
XR_244316.2:n.998+3109G>A
NM_018961.4:c.1046+3109G>A MANE Select NP_061834.1:n.1046+3109G>A
NM_001001895.3:c.932+3109G>A NP_001001895.1:n.932+3109G>A
NM_001243467.2:c.932+3109G>A NP_001230396.1:n.932+3109G>A
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