Canonical Allele Identifier: CA1941765

Gene: TTC21B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165901873T>C , CM000664.2:g.165901873T>C	GRCh38
NC_000002.11:g.166758383T>C , CM000664.1:g.166758383T>C	GRCh37
NC_000002.10:g.166466629T>C	NCBI36
NG_030345.1:g.56966A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000243344.8:c.2606A>G MANE Select	ENSP00000243344.7:p.Gln869Arg
ENST00000652557.1:c.2606A>G	ENSP00000498617.1:p.Gln869Arg
ENST00000679356.1:c.2606A>G	ENSP00000506245.1:p.Gln869Arg
ENST00000679676.1:c.2495A>G	ENSP00000505492.1:p.Gln832Arg
ENST00000679799.1:c.2606A>G	ENSP00000505208.1:p.Gln869Arg
ENST00000679840.1:c.2606A>G	ENSP00000505248.1:p.Gln869Arg
ENST00000679931.1:c.*1648A>G	ENSP00000505632.1:n.*1648A>G
ENST00000679967.1:c.2606A>G	ENSP00000506607.1:p.Gln869Arg
ENST00000680327.1:c.*1648A>G	ENSP00000506639.1:n.*1648A>G
ENST00000680448.1:c.2606A>G	ENSP00000505921.1:p.Gln869Arg
ENST00000680657.1:n.2717A>G
ENST00000680690.1:c.*1858A>G	ENSP00000506121.1:n.*1858A>G
ENST00000680888.1:c.2606A>G	ENSP00000506276.1:p.Gln869Arg
ENST00000680925.1:n.605A>G
ENST00000680947.1:c.*1878A>G	ENSP00000506496.1:n.*1878A>G
ENST00000681024.1:c.2606A>G	ENSP00000506449.1:p.Gln869Arg
ENST00000681083.1:c.*2340A>G	ENSP00000506095.1:n.*2340A>G
ENST00000681167.1:n.2480A>G
ENST00000681483.1:c.2606A>G	ENSP00000505499.1:p.Gln869Arg
ENST00000681502.1:c.*2030A>G	ENSP00000505644.1:n.*2030A>G
ENST00000681606.1:c.2606A>G	ENSP00000505354.1:p.Gln869Arg
ENST00000681819.1:c.2606A>G	ENSP00000505673.1:p.Gln869Arg
ENST00000681952.1:c.2606A>G	ENSP00000506400.1:p.Gln869Arg
ENST00000243344.7:c.2606A>G	ENSP00000243344.7:p.Gln869Arg
ENST00000484129.1:n.81A>G
NM_024753.4:c.2606A>G	NP_079029.3:p.Gln869Arg
XM_006712761.1:c.2606A>G	XP_006712824.1:p.Gln869Arg
XM_011511870.1:c.2039A>G	XP_011510172.1:p.Gln680Arg
XM_011511871.1:c.1856A>G	XP_011510173.1:p.Gln619Arg
XM_011511872.1:c.2606A>G	XP_011510174.1:p.Gln869Arg
XM_011511871.3:c.1856A>G	XP_011510173.1:p.Gln619Arg
XM_011511872.2:c.2606A>G	XP_011510174.1:p.Gln869Arg
XM_017004967.1:c.2606A>G	XP_016860456.1:p.Gln869Arg
XM_017004968.2:c.1952A>G	XP_016860457.1:p.Gln651Arg
XM_017004969.1:c.1607A>G	XP_016860458.1:p.Gln536Arg
NM_024753.5:c.2606A>G MANE Select	NP_079029.3:p.Gln869Arg