Canonical Allele Identifier: CA1941337

Gene: TTC21B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165874791A>T , CM000664.2:g.165874791A>T	GRCh38
NC_000002.11:g.166731301A>T , CM000664.1:g.166731301A>T	GRCh37
NC_000002.10:g.166439547A>T	NCBI36
NG_030345.1:g.84048T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000243344.8:c.3915T>A MANE Select	ENSP00000243344.7:p.Asp1305Glu
ENST00000652557.1:c.3806-3771T>A	ENSP00000498617.1:n.3806-3771T>A
ENST00000679356.1:c.3912T>A	ENSP00000506245.1:p.Asp1304Glu
ENST00000679676.1:c.3804T>A	ENSP00000505492.1:p.Asp1268Glu
ENST00000679799.1:c.3806-3771T>A	ENSP00000505208.1:n.3806-3771T>A
ENST00000679931.1:c.*2957T>A	ENSP00000505632.1:n.*2957T>A
ENST00000679967.1:c.3906T>A	ENSP00000506607.1:p.Asp1302Glu
ENST00000680327.1:c.*2957T>A	ENSP00000506639.1:n.*2957T>A
ENST00000680657.1:n.5358T>A
ENST00000680690.1:c.*3167T>A	ENSP00000506121.1:n.*3167T>A
ENST00000680888.1:c.3915T>A	ENSP00000506276.1:p.Asp1305Glu
ENST00000680904.1:n.419T>A
ENST00000680947.1:c.*3187T>A	ENSP00000506496.1:n.*3187T>A
ENST00000681024.1:c.*3705T>A	ENSP00000506449.1:n.*3705T>A
ENST00000681083.1:c.*3646T>A	ENSP00000506095.1:n.*3646T>A
ENST00000681167.1:n.3793T>A
ENST00000681483.1:c.*725T>A	ENSP00000505499.1:n.*725T>A
ENST00000681502.1:c.*7175T>A	ENSP00000505644.1:n.*7175T>A
ENST00000681819.1:c.*725T>A	ENSP00000505673.1:n.*725T>A
ENST00000681952.1:c.3915T>A	ENSP00000506400.1:p.Asp1305Glu
ENST00000243344.7:c.3915T>A	ENSP00000243344.7:p.Asp1305Glu
ENST00000392695.6:c.815T>A
NM_024753.4:c.3915T>A	NP_079029.3:p.Asp1305Glu
XM_011511870.1:c.3348T>A	XP_011510172.1:p.Asp1116Glu
XM_011511871.1:c.3165T>A	XP_011510173.1:p.Asp1055Glu
XM_011511871.3:c.3165T>A	XP_011510173.1:p.Asp1055Glu
XM_011511872.2:c.*1117T>A	XP_011510174.1:n.*1117T>A
XM_017004968.2:c.3261T>A	XP_016860457.1:p.Asp1087Glu
XM_017004969.1:c.2916T>A	XP_016860458.1:p.Asp972Glu
NM_024753.5:c.3915T>A MANE Select	NP_079029.3:p.Asp1305Glu