Canonical Allele Identifier: CA357821853
Gene: TBCK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.106230383T>G , CM000666.2:g.106230383T>G GRCh38
NC_000004.11:g.107151540T>G , CM000666.1:g.107151540T>G GRCh37
NC_000004.10:g.107370989T>G NCBI36
NG_034057.2:g.96113A>C
NG_034057.3:g.91301A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000273980.10:c.1754A>C ENSP00000273980.4:p.Asp585Ala
ENST00000394708.7:c.1754A>C MANE Select ENSP00000378198.2:p.Asp585Ala
ENST00000273980.9:c.1754A>C ENSP00000273980.4:p.Asp585Ala
ENST00000361687.8:c.1565A>C ENSP00000355338.4:p.Asp522Ala
ENST00000394706.7:c.1637A>C ENSP00000378196.3:p.Asp546Ala
ENST00000394708.6:c.1754A>C ENSP00000378198.2:p.Asp585Ala
ENST00000432496.6:c.1754A>C ENSP00000405847.2:p.Asp585Ala
ENST00000467183.6:c.*1393A>C ENSP00000421182.1:n.*1393A>C
ENST00000506615.1:n.64A>C
ENST00000510927.5:n.1407A>C
NM_001163435.2:c.1754A>C NP_001156907.1:p.Asp585Ala
NM_001163436.2:c.1754A>C NP_001156908.1:p.Asp585Ala
NM_001163437.2:c.1637A>C NP_001156909.1:p.Asp546Ala
NM_001290768.1:c.1238A>C NP_001277697.1:p.Asp413Ala
NM_033115.4:c.1565A>C NP_149106.2:p.Asp522Ala
XM_006714419.2:c.1754A>C XP_006714482.1:p.Asp585Ala
XM_011532417.1:c.1754A>C XP_011530719.1:p.Asp585Ala
XM_011532418.1:c.1436A>C XP_011530720.1:p.Asp479Ala
XM_011532419.1:c.1238A>C XP_011530721.1:p.Asp413Ala
XR_938800.1:n.1783A>C
XM_011532417.2:c.1754A>C XP_011530719.1:p.Asp585Ala
XM_017008846.1:c.1754A>C XP_016864335.1:p.Asp585Ala
XM_017008847.2:c.1754A>C XP_016864336.1:p.Asp585Ala
XM_017008848.1:c.1436A>C XP_016864337.1:p.Asp479Ala
XM_017008849.1:c.1238A>C XP_016864338.1:p.Asp413Ala
XM_024454281.1:c.1754A>C XP_024310049.1:p.Asp585Ala
XM_024454282.1:c.1754A>C XP_024310050.1:p.Asp585Ala
XR_001741353.2:n.2094A>C
XR_001741354.2:n.1691A>C
XR_002959772.1:n.1878A>C
XR_938800.3:n.2094A>C
NM_001163435.3:c.1754A>C MANE Select NP_001156907.2:p.Asp585Ala
NM_001163436.4:c.1754A>C NP_001156908.2:p.Asp585Ala
NM_001163437.3:c.1637A>C NP_001156909.2:p.Asp546Ala
NM_001290768.2:c.1238A>C NP_001277697.2:p.Asp413Ala
NM_033115.5:c.1565A>C NP_149106.3:p.Asp522Ala