Canonical Allele Identifier: CA1942387

Gene: TTC21B TTC21B-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165941162T>C , CM000664.2:g.165941162T>C	GRCh38
NC_000002.11:g.166797672T>C , CM000664.1:g.166797672T>C	GRCh37
NC_000002.10:g.166505918T>C	NCBI36
NG_030345.1:g.17677A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_024753.5:c.575A>G (TTC21B) MANE Select	NP_079029.3:p.Gln192Arg
ENST00000243344.8:c.575A>G (TTC21B) MANE Select	ENSP00000243344.7:p.Gln192Arg
NM_024753.4:c.575A>G (TTC21B)	NP_079029.3:p.Gln192Arg
NR_038983.1:n.277-6035T>C (TTC21B-AS1)
NR_038984.1:n.221-6035T>C (TTC21B-AS1)
ENST00000243344.7:c.575A>G (TTC21B)	ENSP00000243344.7:p.Gln192Arg
ENST00000464374.5:n.615A>G (TTC21B)
ENST00000652557.1:c.575A>G (TTC21B)	ENSP00000498617.1:p.Gln192Arg
ENST00000679356.1:c.575A>G (TTC21B)	ENSP00000506245.1:p.Gln192Arg
ENST00000679671.1:n.688A>G (TTC21B)
ENST00000679676.1:c.464A>G (TTC21B)	ENSP00000505492.1:p.Gln155Arg
ENST00000679799.1:c.575A>G (TTC21B)	ENSP00000505208.1:p.Gln192Arg
ENST00000679840.1:c.575A>G (TTC21B)	ENSP00000505248.1:p.Gln192Arg
ENST00000679931.1:c.575A>G (TTC21B)	ENSP00000505632.1:p.Gln192Arg
ENST00000679967.1:c.575A>G (TTC21B)	ENSP00000506607.1:p.Gln192Arg
ENST00000680327.1:c.575A>G (TTC21B)	ENSP00000506639.1:p.Gln192Arg
ENST00000680448.1:c.575A>G (TTC21B)	ENSP00000505921.1:p.Gln192Arg
ENST00000680657.1:n.686A>G (TTC21B)
ENST00000680690.1:c.575A>G (TTC21B)	ENSP00000506121.1:p.Gln192Arg
ENST00000680888.1:c.575A>G (TTC21B)	ENSP00000506276.1:p.Gln192Arg
ENST00000680947.1:c.552+2057A>G (TTC21B)	ENSP00000506496.1:n.552+2057A>G
ENST00000681024.1:c.575A>G (TTC21B)	ENSP00000506449.1:p.Gln192Arg
ENST00000681083.1:c.*309A>G (TTC21B)	ENSP00000506095.1:n.*309A>G
ENST00000681483.1:c.575A>G (TTC21B)	ENSP00000505499.1:p.Gln192Arg
ENST00000681502.1:c.575A>G (TTC21B)	ENSP00000505644.1:p.Gln192Arg
ENST00000681606.1:c.575A>G (TTC21B)	ENSP00000505354.1:p.Gln192Arg
ENST00000681819.1:c.575A>G (TTC21B)	ENSP00000505673.1:p.Gln192Arg
ENST00000681952.1:c.575A>G (TTC21B)	ENSP00000506400.1:p.Gln192Arg
XM_006712761.1:c.575A>G (TTC21B)	XP_006712824.1:p.Gln192Arg
XM_011511870.1:c.8A>G (TTC21B)	XP_011510172.1:p.Gln3Arg
XM_011511872.1:c.575A>G (TTC21B)	XP_011510174.1:p.Gln192Arg
XM_011511872.2:c.575A>G (TTC21B)	XP_011510174.1:p.Gln192Arg
XM_017004967.1:c.575A>G (TTC21B)	XP_016860456.1:p.Gln192Arg
XM_017004969.1:c.-442A>G (TTC21B)	XP_016860458.1:n.-442A>G