Canonical Allele Identifier: CA1941424

Gene: TTC21B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165880782A>G , CM000664.2:g.165880782A>G	GRCh38
NC_000002.11:g.166737292A>G , CM000664.1:g.166737292A>G	GRCh37
NC_000002.10:g.166445538A>G	NCBI36
NG_030345.1:g.78057T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_024753.5:c.3702T>C MANE Select	NP_079029.3:p.Tyr1234=
ENST00000243344.8:c.3702T>C MANE Select	ENSP00000243344.7:p.Tyr1234=
NM_024753.4:c.3702T>C	NP_079029.3:p.Tyr1234=
ENST00000243344.7:c.3702T>C	ENSP00000243344.7:p.Tyr1234=
ENST00000392695.6:c.602T>C
ENST00000497425.1:n.180T>C
ENST00000497425.2:n.811T>C
ENST00000652557.1:c.3702T>C	ENSP00000498617.1:p.Tyr1234=
ENST00000679356.1:c.3699T>C	ENSP00000506245.1:p.Tyr1233=
ENST00000679676.1:c.3591T>C	ENSP00000505492.1:p.Tyr1197=
ENST00000679799.1:c.3702T>C	ENSP00000505208.1:p.Tyr1234=
ENST00000679840.1:c.3702T>C	ENSP00000505248.1:p.Tyr1234=
ENST00000679931.1:c.*2744T>C	ENSP00000505632.1:n.*2744T>C
ENST00000679967.1:c.3693T>C	ENSP00000506607.1:p.Tyr1231=
ENST00000680327.1:c.*2744T>C	ENSP00000506639.1:n.*2744T>C
ENST00000680657.1:n.3813T>C
ENST00000680690.1:c.*2954T>C	ENSP00000506121.1:n.*2954T>C
ENST00000680888.1:c.3702T>C	ENSP00000506276.1:p.Tyr1234=
ENST00000680925.1:n.1732T>C
ENST00000680947.1:c.*2974T>C	ENSP00000506496.1:n.*2974T>C
ENST00000681024.1:c.3702T>C	ENSP00000506449.1:p.Tyr1234=
ENST00000681083.1:c.*3433T>C	ENSP00000506095.1:n.*3433T>C
ENST00000681167.1:n.3580T>C
ENST00000681483.1:c.*512T>C	ENSP00000505499.1:n.*512T>C
ENST00000681502.1:c.*6962T>C	ENSP00000505644.1:n.*6962T>C
ENST00000681819.1:c.*512T>C	ENSP00000505673.1:n.*512T>C
ENST00000681952.1:c.3702T>C	ENSP00000506400.1:p.Tyr1234=
XM_011511870.1:c.3135T>C	XP_011510172.1:p.Tyr1045=
XM_011511871.1:c.2952T>C	XP_011510173.1:p.Tyr984=
XM_011511871.3:c.2952T>C	XP_011510173.1:p.Tyr984=
XM_011511872.2:c.*904T>C	XP_011510174.1:n.*904T>C
XM_017004967.1:c.3702T>C	XP_016860456.1:p.Tyr1234=
XM_017004968.2:c.3048T>C	XP_016860457.1:p.Tyr1016=
XM_017004969.1:c.2703T>C	XP_016860458.1:p.Tyr901=