Canonical Allele Identifier: CA14863459
Gene: UBASH3A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.42416281A>G , CM000683.2:g.42416281A>G GRCh38
NC_000021.8:g.43836390A>G , CM000683.1:g.43836390A>G GRCh37
NC_000021.7:g.42709459A>G NCBI36
NG_029750.1:g.17420A>G
NG_029750.2:g.17420A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000319294.11:c.668-161A>G MANE Select ENSP00000317327.6:n.668-161A>G
ENST00000291535.11:c.554-161A>G ENSP00000291535.6:n.554-161A>G
ENST00000319294.10:c.668-161A>G ENSP00000317327.6:n.668-161A>G
ENST00000398367.1:c.554-161A>G ENSP00000381408.1:n.554-161A>G
ENST00000473381.1:c.554-161A>G ENSP00000489235.1:n.554-161A>G
ENST00000635325.1:c.554-161A>G ENSP00000489463.1:n.554-161A>G
NM_001001895.2:c.554-161A>G NP_001001895.1:n.554-161A>G
NM_001243467.1:c.554-161A>G NP_001230396.1:n.554-161A>G
NM_018961.3:c.668-161A>G NP_061834.1:n.668-161A>G
XM_006724013.2:c.611-161A>G XP_006724076.1:n.611-161A>G
XM_011529605.1:c.668-161A>G XP_011527907.1:n.668-161A>G
XM_011529606.1:c.263-161A>G XP_011527908.1:n.263-161A>G
XM_011529607.1:c.263-161A>G XP_011527909.1:n.263-161A>G
XM_011529608.1:c.668-161A>G XP_011527910.1:n.668-161A>G
XM_011529609.1:c.668-161A>G XP_011527911.1:n.668-161A>G
XM_011529610.1:c.-177A>G XP_011527912.1:n.-177A>G
XR_244316.1:n.638-161A>G
XR_937510.1:n.638-161A>G
XM_006724013.3:c.611-161A>G XP_006724076.1:n.611-161A>G
XM_011529605.3:c.668-161A>G XP_011527907.1:n.668-161A>G
XM_011529606.3:c.263-161A>G XP_011527908.1:n.263-161A>G
XM_011529607.2:c.263-161A>G XP_011527909.1:n.263-161A>G
XM_011529609.2:c.668-161A>G XP_011527911.1:n.668-161A>G
XM_011529610.2:c.-177A>G XP_011527912.1:n.-177A>G
XR_244316.2:n.620-161A>G
NM_018961.4:c.668-161A>G MANE Select NP_061834.1:n.668-161A>G
NM_001001895.3:c.554-161A>G NP_001001895.1:n.554-161A>G
NM_001243467.2:c.554-161A>G NP_001230396.1:n.554-161A>G
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