Canonical Allele Identifier: CA400511008

Gene: TLK2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.62600736C>T , CM000679.2:g.62600736C>T	GRCh38
NC_000017.10:g.60678097C>T , CM000679.1:g.60678097C>T	GRCh37
NC_000017.9:g.58031829C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682075.1:c.1372C>T	ENSP00000506988.1:p.Arg458Trp
ENST00000682085.1:c.1636C>T	ENSP00000506744.1:p.Arg546Trp
ENST00000682203.1:c.1189C>T	ENSP00000507584.1:p.Arg397Trp
ENST00000682274.1:c.*1157C>T	ENSP00000507636.1:n.*1157C>T
ENST00000683104.1:c.1540C>T	ENSP00000508242.1:p.Arg514Trp
ENST00000683536.1:c.1189C>T	ENSP00000508315.1:p.Arg397Trp
ENST00000683737.1:n.3064C>T
ENST00000684012.1:c.1447C>T	ENSP00000507902.1:p.Arg483Trp
ENST00000684133.1:n.1046C>T
ENST00000684440.1:c.1447C>T	ENSP00000507712.1:p.Arg483Trp
ENST00000684553.1:c.1429C>T	ENSP00000507681.1:p.Arg477Trp
ENST00000684772.1:c.1351C>T	ENSP00000507724.1:p.Arg451Trp
ENST00000346027.10:c.1636C>T MANE Select	ENSP00000275780.7:p.Arg546Trp
ENST00000326270.13:c.1702C>T	ENSP00000316512.9:p.Arg568Trp
ENST00000343388.11:c.1540C>T	ENSP00000340800.7:p.Arg514Trp
ENST00000346027.9:c.1636C>T	ENSP00000275780.7:p.Arg546Trp
ENST00000578931.1:n.315+144C>T
ENST00000581041.5:c.1444C>T	ENSP00000462036.1:p.Arg482Trp
ENST00000582660.1:n.846C>T
ENST00000582809.5:c.1189C>T	ENSP00000463595.1:p.Arg397Trp
NM_001284333.1:c.1702C>T	NP_001271262.1:p.Arg568Trp
NM_001284363.1:c.1540C>T	NP_001271292.1:p.Arg514Trp
NM_006852.3:c.1636C>T	NP_006843.2:p.Arg546Trp
XM_011524215.1:c.1609C>T	XP_011522517.1:p.Arg537Trp
XM_011524216.1:c.1702C>T	XP_011522518.1:p.Arg568Trp
XM_011524217.1:c.1702C>T	XP_011522519.1:p.Arg568Trp
XM_011524218.1:c.1543C>T	XP_011522520.1:p.Arg515Trp
XM_011524219.1:c.1540C>T	XP_011522521.1:p.Arg514Trp
XM_011524220.1:c.1513C>T	XP_011522522.1:p.Arg505Trp
XM_011524221.1:c.1606C>T	XP_011522523.1:p.Arg536Trp
XM_011524222.1:c.1702C>T	XP_011522524.1:p.Arg568Trp
XM_011524223.1:c.1513C>T	XP_011522525.1:p.Arg505Trp
XM_011524224.1:c.1390C>T	XP_011522526.1:p.Arg464Trp
XM_011524225.1:c.1390C>T	XP_011522527.1:p.Arg464Trp
XM_011524226.1:c.1390C>T	XP_011522528.1:p.Arg464Trp
XM_011524227.1:c.1390C>T	XP_011522529.1:p.Arg464Trp
XM_011524228.1:c.1390C>T	XP_011522530.1:p.Arg464Trp
XM_011524229.1:c.1255C>T	XP_011522531.1:p.Arg419Trp
XM_011524230.1:c.1189C>T	XP_011522532.1:p.Arg397Trp
NM_001330418.1:c.1189C>T	NP_001317347.1:p.Arg397Trp
XM_011524215.2:c.1609C>T	XP_011522517.1:p.Arg537Trp
XM_011524216.2:c.1702C>T	XP_011522518.1:p.Arg568Trp
XM_011524217.3:c.1702C>T	XP_011522519.1:p.Arg568Trp
XM_011524218.2:c.1543C>T	XP_011522520.1:p.Arg515Trp
XM_011524220.2:c.1513C>T	XP_011522522.1:p.Arg505Trp
XM_011524221.2:c.1606C>T	XP_011522523.1:p.Arg536Trp
XM_011524222.3:c.1702C>T	XP_011522524.1:p.Arg568Trp
XM_011524223.3:c.1513C>T	XP_011522525.1:p.Arg505Trp
XM_011524224.3:c.1390C>T	XP_011522526.1:p.Arg464Trp
XM_011524225.3:c.1390C>T	XP_011522527.1:p.Arg464Trp
XM_011524226.2:c.1390C>T	XP_011522528.1:p.Arg464Trp
XM_011524227.2:c.1390C>T	XP_011522529.1:p.Arg464Trp
XM_011524228.3:c.1390C>T	XP_011522530.1:p.Arg464Trp
XM_011524229.2:c.1255C>T	XP_011522531.1:p.Arg419Trp
XM_017024044.1:c.1636C>T	XP_016879533.1:p.Arg546Trp
XM_017024045.1:c.1678C>T	XP_016879534.1:p.Arg560Trp
XM_017024046.1:c.1636C>T	XP_016879535.1:p.Arg546Trp
XM_017024047.1:c.1636C>T	XP_016879536.1:p.Arg546Trp
XM_017024048.2:c.1606C>T	XP_016879537.1:p.Arg536Trp
XM_017024049.2:c.1606C>T	XP_016879538.1:p.Arg536Trp
XM_017024050.1:c.1585C>T	XP_016879539.1:p.Arg529Trp
XM_017024051.2:c.1540C>T	XP_016879540.1:p.Arg514Trp
XM_017024052.2:c.1540C>T	XP_016879541.1:p.Arg514Trp
XM_017024053.2:c.1540C>T	XP_016879542.1:p.Arg514Trp
XM_017024054.2:c.1447C>T	XP_016879543.1:p.Arg483Trp
XM_017024055.2:c.1351C>T	XP_016879544.1:p.Arg451Trp
XM_017024056.2:c.1324C>T	XP_016879545.1:p.Arg442Trp
XM_017024057.1:c.1324C>T	XP_016879546.1:p.Arg442Trp
XM_017024059.1:c.1189C>T	XP_016879548.1:p.Arg397Trp
XM_017024060.1:c.1000C>T	XP_016879549.1:p.Arg334Trp
XM_024450552.1:c.1723C>T	XP_024306320.1:p.Arg575Trp
XM_024450553.1:c.1702C>T	XP_024306321.1:p.Arg568Trp
NM_001284333.2:c.1702C>T	NP_001271262.1:p.Arg568Trp
NM_001330418.2:c.1189C>T	NP_001317347.1:p.Arg397Trp
NM_001375269.1:c.1678C>T	NP_001362198.1:p.Arg560Trp
NM_001375270.1:c.1636C>T	NP_001362199.1:p.Arg546Trp
NM_001375271.1:c.1636C>T	NP_001362200.1:p.Arg546Trp
NM_001375272.1:c.1540C>T	NP_001362201.1:p.Arg514Trp
NM_001375273.1:c.1189C>T	NP_001362202.1:p.Arg397Trp
NM_006852.6:c.1636C>T MANE Select	NP_006843.2:p.Arg546Trp
NM_001284333.3:c.1702C>T	NP_001271262.1:p.Arg568Trp
NM_001330418.3:c.1189C>T	NP_001317347.1:p.Arg397Trp