Canonical Allele Identifier: CA340548493
Gene: PATJ HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.61914642A>C , CM000663.2:g.61914642A>C GRCh38
NC_000001.10:g.62380314A>C , CM000663.1:g.62380314A>C GRCh37
NC_000001.9:g.62152902A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642238.2:c.3548A>C MANE Select ENSP00000494277.1:p.Asp1183Ala
ENST00000316485.11:c.3491-3382A>C ENSP00000326199.7:n.3491-3382A>C
ENST00000371158.6:c.3548A>C ENSP00000360200.2:p.Asp1183Ala
ENST00000459752.5:n.3662A>C
ENST00000484562.5:n.3662A>C
ENST00000484937.5:c.1925A>C ENSP00000433669.1:p.Asp642Ala
ENST00000494842.2:c.84A>C
ENST00000613764.4:c.3381+13183A>C ENSP00000479041.1:n.3381+13183A>C
ENST00000635023.1:c.*1516A>C ENSP00000489335.1:n.*1516A>C
ENST00000635214.1:n.3662A>C
NM_176877.2:c.3548A>C NP_795352.2:p.Asp1183Ala
XM_005270341.2:c.3548A>C XP_005270398.1:p.Asp1183Ala
XM_005270347.1:c.3548A>C XP_005270404.1:p.Asp1183Ala
XM_006710278.2:c.3548A>C XP_006710341.1:p.Asp1183Ala
XM_011540462.1:c.3548A>C XP_011538764.1:p.Asp1183Ala
XM_011540463.1:c.3548A>C XP_011538765.1:p.Asp1183Ala
XM_011540464.1:c.3548A>C XP_011538766.1:p.Asp1183Ala
XM_011540465.1:c.3548A>C XP_011538767.1:p.Asp1183Ala
XM_011540466.1:c.3548A>C XP_011538768.1:p.Asp1183Ala
XM_011540467.1:c.3548A>C XP_011538769.1:p.Asp1183Ala
XM_011540468.1:c.3548A>C XP_011538770.1:p.Asp1183Ala
XM_011540469.1:c.3548A>C XP_011538771.1:p.Asp1183Ala
NM_001350145.1:c.3548A>C NP_001337074.1:p.Asp1183Ala
NM_176877.3:c.3548A>C NP_795352.2:p.Asp1183Ala
XM_005270347.2:c.3548A>C XP_005270404.1:p.Asp1183Ala
XM_006710278.4:c.3548A>C XP_006710341.1:p.Asp1183Ala
XM_011540462.3:c.3548A>C XP_011538764.1:p.Asp1183Ala
XM_011540463.2:c.3548A>C XP_011538765.1:p.Asp1183Ala
XM_011540464.3:c.3548A>C XP_011538766.1:p.Asp1183Ala
XM_011540465.3:c.3548A>C XP_011538767.1:p.Asp1183Ala
XM_011540466.3:c.3548A>C XP_011538768.1:p.Asp1183Ala
XM_011540467.3:c.3548A>C XP_011538769.1:p.Asp1183Ala
XM_011540468.3:c.3548A>C XP_011538770.1:p.Asp1183Ala
XM_011540469.3:c.3548A>C XP_011538771.1:p.Asp1183Ala
XM_016999998.2:c.3548A>C XP_016855487.1:p.Asp1183Ala
XM_016999999.2:c.3548A>C XP_016855488.1:p.Asp1183Ala
XM_017000000.1:c.2639A>C XP_016855489.1:p.Asp880Ala
XM_017000001.1:c.713A>C XP_016855490.1:p.Asp238Ala
XM_024448614.1:c.3548A>C XP_024304382.1:p.Asp1183Ala
XM_024448642.1:c.3548A>C XP_024304410.1:p.Asp1183Ala
XR_001736900.2:n.3662A>C
XR_002957157.1:n.3662A>C
NM_001350145.3:c.3548A>C MANE Select NP_001337074.2:p.Asp1183Ala
NM_176877.5:c.3548A>C NP_795352.3:p.Asp1183Ala