Canonical Allele Identifier: CA429891976

Gene: TTC21B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165874797T>C , CM000664.2:g.165874797T>C	GRCh38
NC_000002.11:g.166731307T>C , CM000664.1:g.166731307T>C	GRCh37
NC_000002.10:g.166439553T>C	NCBI36
NG_030345.1:g.84042A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_024753.5:c.3909A>G MANE Select	NP_079029.3:p.Arg1303=
ENST00000243344.8:c.3909A>G MANE Select	ENSP00000243344.7:p.Arg1303=
NM_024753.4:c.3909A>G	NP_079029.3:p.Arg1303=
ENST00000243344.7:c.3909A>G	ENSP00000243344.7:p.Arg1303=
ENST00000392695.6:c.809A>G
ENST00000652557.1:c.3806-3777A>G	ENSP00000498617.1:n.3806-3777A>G
ENST00000679356.1:c.3906A>G	ENSP00000506245.1:p.Arg1302=
ENST00000679676.1:c.3798A>G	ENSP00000505492.1:p.Arg1266=
ENST00000679799.1:c.3806-3777A>G	ENSP00000505208.1:n.3806-3777A>G
ENST00000679931.1:c.*2951A>G	ENSP00000505632.1:n.*2951A>G
ENST00000679967.1:c.3900A>G	ENSP00000506607.1:p.Arg1300=
ENST00000680327.1:c.*2951A>G	ENSP00000506639.1:n.*2951A>G
ENST00000680657.1:n.5352A>G
ENST00000680690.1:c.*3161A>G	ENSP00000506121.1:n.*3161A>G
ENST00000680888.1:c.3909A>G	ENSP00000506276.1:p.Arg1303=
ENST00000680904.1:n.413A>G
ENST00000680947.1:c.*3181A>G	ENSP00000506496.1:n.*3181A>G
ENST00000681024.1:c.*3699A>G	ENSP00000506449.1:n.*3699A>G
ENST00000681083.1:c.*3640A>G	ENSP00000506095.1:n.*3640A>G
ENST00000681167.1:n.3787A>G
ENST00000681483.1:c.*719A>G	ENSP00000505499.1:n.*719A>G
ENST00000681502.1:c.*7169A>G	ENSP00000505644.1:n.*7169A>G
ENST00000681819.1:c.*719A>G	ENSP00000505673.1:n.*719A>G
ENST00000681952.1:c.3909A>G	ENSP00000506400.1:p.Arg1303=
XM_011511870.1:c.3342A>G	XP_011510172.1:p.Arg1114=
XM_011511871.1:c.3159A>G	XP_011510173.1:p.Arg1053=
XM_011511871.3:c.3159A>G	XP_011510173.1:p.Arg1053=
XM_011511872.2:c.*1111A>G	XP_011510174.1:n.*1111A>G
XM_017004968.2:c.3255A>G	XP_016860457.1:p.Arg1085=
XM_017004969.1:c.2910A>G	XP_016860458.1:p.Arg970=