Canonical Allele Identifier: CA1941343

Gene: TTC21B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165874814T>C , CM000664.2:g.165874814T>C	GRCh38
NC_000002.11:g.166731324T>C , CM000664.1:g.166731324T>C	GRCh37
NC_000002.10:g.166439570T>C	NCBI36
NG_030345.1:g.84025A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_024753.5:c.3892A>G MANE Select	NP_079029.3:p.Thr1298Ala
ENST00000243344.8:c.3892A>G MANE Select	ENSP00000243344.7:p.Thr1298Ala
NM_024753.4:c.3892A>G	NP_079029.3:p.Thr1298Ala
ENST00000243344.7:c.3892A>G	ENSP00000243344.7:p.Thr1298Ala
ENST00000392695.6:c.792A>G
ENST00000652557.1:c.3806-3794A>G	ENSP00000498617.1:n.3806-3794A>G
ENST00000679356.1:c.3889A>G	ENSP00000506245.1:p.Thr1297Ala
ENST00000679676.1:c.3781A>G	ENSP00000505492.1:p.Thr1261Ala
ENST00000679799.1:c.3806-3794A>G	ENSP00000505208.1:n.3806-3794A>G
ENST00000679931.1:c.*2934A>G	ENSP00000505632.1:n.*2934A>G
ENST00000679967.1:c.3883A>G	ENSP00000506607.1:p.Thr1295Ala
ENST00000680327.1:c.*2934A>G	ENSP00000506639.1:n.*2934A>G
ENST00000680657.1:n.5335A>G
ENST00000680690.1:c.*3144A>G	ENSP00000506121.1:n.*3144A>G
ENST00000680888.1:c.3892A>G	ENSP00000506276.1:p.Thr1298Ala
ENST00000680904.1:n.396A>G
ENST00000680947.1:c.*3164A>G	ENSP00000506496.1:n.*3164A>G
ENST00000681024.1:c.*3682A>G	ENSP00000506449.1:n.*3682A>G
ENST00000681083.1:c.*3623A>G	ENSP00000506095.1:n.*3623A>G
ENST00000681167.1:n.3770A>G
ENST00000681483.1:c.*702A>G	ENSP00000505499.1:n.*702A>G
ENST00000681502.1:c.*7152A>G	ENSP00000505644.1:n.*7152A>G
ENST00000681819.1:c.*702A>G	ENSP00000505673.1:n.*702A>G
ENST00000681952.1:c.3892A>G	ENSP00000506400.1:p.Thr1298Ala
XM_011511870.1:c.3325A>G	XP_011510172.1:p.Thr1109Ala
XM_011511871.1:c.3142A>G	XP_011510173.1:p.Thr1048Ala
XM_011511871.3:c.3142A>G	XP_011510173.1:p.Thr1048Ala
XM_011511872.2:c.*1094A>G	XP_011510174.1:n.*1094A>G
XM_017004968.2:c.3238A>G	XP_016860457.1:p.Thr1080Ala
XM_017004969.1:c.2893A>G	XP_016860458.1:p.Thr965Ala