Canonical Allele Identifier: CA59795496

Gene: TTC21B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165911008_165911010del , CM000664.2:g.165911008_165911010del	GRCh38
NC_000002.11:g.166767518_166767520del , CM000664.1:g.166767518_166767520del	GRCh37
NC_000002.10:g.166475764_166475766del	NCBI36
NG_030345.1:g.47832_47834del

Transcript Alleles

HGVS	Amino-acid Change
NM_024753.5:c.2461+320_2461+322del MANE Select	NP_079029.3:n.2461+320_2461+322del
ENST00000243344.8:c.2461+320_2461+322del MANE Select	ENSP00000243344.7:n.2461+320_2461+322del
NM_024753.4:c.2461+320_2461+322del	NP_079029.3:n.2461+320_2461+322del
ENST00000243344.7:c.2461+320_2461+322del	ENSP00000243344.7:n.2461+320_2461+322del
ENST00000652557.1:c.2461+320_2461+322del	ENSP00000498617.1:n.2461+320_2461+322del
ENST00000679356.1:c.2461+320_2461+322del	ENSP00000506245.1:n.2461+320_2461+322del
ENST00000679671.1:n.2894_2896del
ENST00000679676.1:c.2350+320_2350+322del	ENSP00000505492.1:n.2350+320_2350+322del
ENST00000679799.1:c.2461+320_2461+322del	ENSP00000505208.1:n.2461+320_2461+322del
ENST00000679840.1:c.2461+320_2461+322del	ENSP00000505248.1:n.2461+320_2461+322del
ENST00000679931.1:c.*1503+320_*1503+322del	ENSP00000505632.1:n.*1503+320_*1503+322del
ENST00000679967.1:c.2461+320_2461+322del	ENSP00000506607.1:n.2461+320_2461+322del
ENST00000680327.1:c.*1503+320_*1503+322del	ENSP00000506639.1:n.*1503+320_*1503+322del
ENST00000680448.1:c.2461+320_2461+322del	ENSP00000505921.1:n.2461+320_2461+322del
ENST00000680657.1:n.2572+320_2572+322del
ENST00000680690.1:c.*1713+320_*1713+322del	ENSP00000506121.1:n.*1713+320_*1713+322del
ENST00000680888.1:c.2461+320_2461+322del	ENSP00000506276.1:n.2461+320_2461+322del
ENST00000680947.1:c.*1733+320_*1733+322del	ENSP00000506496.1:n.*1733+320_*1733+322del
ENST00000681024.1:c.2461+320_2461+322del	ENSP00000506449.1:n.2461+320_2461+322del
ENST00000681083.1:c.*2195+320_*2195+322del	ENSP00000506095.1:n.*2195+320_*2195+322del
ENST00000681167.1:n.2335+320_2335+322del
ENST00000681483.1:c.2461+320_2461+322del	ENSP00000505499.1:n.2461+320_2461+322del
ENST00000681502.1:c.*1885+320_*1885+322del	ENSP00000505644.1:n.*1885+320_*1885+322del
ENST00000681606.1:c.2461+320_2461+322del	ENSP00000505354.1:n.2461+320_2461+322del
ENST00000681819.1:c.2461+320_2461+322del	ENSP00000505673.1:n.2461+320_2461+322del
ENST00000681952.1:c.2461+320_2461+322del	ENSP00000506400.1:n.2461+320_2461+322del
XM_006712761.1:c.2461+320_2461+322del	XP_006712824.1:n.2461+320_2461+322del
XM_011511870.1:c.1894+320_1894+322del	XP_011510172.1:n.1894+320_1894+322del
XM_011511871.1:c.1711+320_1711+322del	XP_011510173.1:n.1711+320_1711+322del
XM_011511871.3:c.1711+320_1711+322del	XP_011510173.1:n.1711+320_1711+322del
XM_011511872.1:c.2461+320_2461+322del	XP_011510174.1:n.2461+320_2461+322del
XM_011511872.2:c.2461+320_2461+322del	XP_011510174.1:n.2461+320_2461+322del
XM_017004967.1:c.2461+320_2461+322del	XP_016860456.1:n.2461+320_2461+322del
XM_017004968.2:c.1807+320_1807+322del	XP_016860457.1:n.1807+320_1807+322del
XM_017004969.1:c.1462+320_1462+322del	XP_016860458.1:n.1462+320_1462+322del