Canonical Allele Identifier: CA1942514

Gene: TTC21B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165949421A>G , CM000664.2:g.165949421A>G	GRCh38
NC_000002.11:g.166805931A>G , CM000664.1:g.166805931A>G	GRCh37
NC_000002.10:g.166514177A>G	NCBI36
NG_030345.1:g.9418T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_024753.5:c.235T>C MANE Select	NP_079029.3:p.Tyr79His
ENST00000243344.8:c.235T>C MANE Select	ENSP00000243344.7:p.Tyr79His
NM_024753.4:c.235T>C	NP_079029.3:p.Tyr79His
ENST00000243344.7:c.235T>C	ENSP00000243344.7:p.Tyr79His
ENST00000464374.5:n.275T>C
ENST00000476227.1:n.341T>C
ENST00000652557.1:c.235T>C	ENSP00000498617.1:p.Tyr79His
ENST00000679356.1:c.235T>C	ENSP00000506245.1:p.Tyr79His
ENST00000679671.1:n.348T>C
ENST00000679676.1:c.151+174T>C	ENSP00000505492.1:n.151+174T>C
ENST00000679799.1:c.235T>C	ENSP00000505208.1:p.Tyr79His
ENST00000679840.1:c.235T>C	ENSP00000505248.1:p.Tyr79His
ENST00000679931.1:c.235T>C	ENSP00000505632.1:p.Tyr79His
ENST00000679967.1:c.235T>C	ENSP00000506607.1:p.Tyr79His
ENST00000680327.1:c.235T>C	ENSP00000506639.1:p.Tyr79His
ENST00000680448.1:c.235T>C	ENSP00000505921.1:p.Tyr79His
ENST00000680657.1:n.346T>C
ENST00000680690.1:c.235T>C	ENSP00000506121.1:p.Tyr79His
ENST00000680888.1:c.235T>C	ENSP00000506276.1:p.Tyr79His
ENST00000680947.1:c.235T>C	ENSP00000506496.1:p.Tyr79His
ENST00000681024.1:c.235T>C	ENSP00000506449.1:p.Tyr79His
ENST00000681083.1:c.235T>C	ENSP00000506095.1:p.Tyr79His
ENST00000681483.1:c.235T>C	ENSP00000505499.1:p.Tyr79His
ENST00000681502.1:c.235T>C	ENSP00000505644.1:p.Tyr79His
ENST00000681606.1:c.235T>C	ENSP00000505354.1:p.Tyr79His
ENST00000681819.1:c.235T>C	ENSP00000505673.1:p.Tyr79His
ENST00000681952.1:c.235T>C	ENSP00000506400.1:p.Tyr79His
XM_006712761.1:c.235T>C	XP_006712824.1:p.Tyr79His
XM_011511870.1:c.-166T>C	XP_011510172.1:n.-166T>C
XM_011511872.1:c.235T>C	XP_011510174.1:p.Tyr79His
XM_011511872.2:c.235T>C	XP_011510174.1:p.Tyr79His
XM_017004967.1:c.235T>C	XP_016860456.1:p.Tyr79His
XM_017004969.1:c.-782T>C	XP_016860458.1:n.-782T>C