Canonical Allele Identifier: CA349057099

Gene: TTC21B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165911432C>G , CM000664.2:g.165911432C>G	GRCh38
NC_000002.11:g.166767942C>G , CM000664.1:g.166767942C>G	GRCh37
NC_000002.10:g.166476188C>G	NCBI36
NG_030345.1:g.47407G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_024753.5:c.2356G>C MANE Select	NP_079029.3:p.Gly786Arg
ENST00000243344.8:c.2356G>C MANE Select	ENSP00000243344.7:p.Gly786Arg
NM_024753.4:c.2356G>C	NP_079029.3:p.Gly786Arg
ENST00000243344.7:c.2356G>C	ENSP00000243344.7:p.Gly786Arg
ENST00000652557.1:c.2356G>C	ENSP00000498617.1:p.Gly786Arg
ENST00000679356.1:c.2356G>C	ENSP00000506245.1:p.Gly786Arg
ENST00000679671.1:n.2469G>C
ENST00000679676.1:c.2245G>C	ENSP00000505492.1:p.Gly749Arg
ENST00000679799.1:c.2356G>C	ENSP00000505208.1:p.Gly786Arg
ENST00000679840.1:c.2356G>C	ENSP00000505248.1:p.Gly786Arg
ENST00000679931.1:c.*1398G>C	ENSP00000505632.1:n.*1398G>C
ENST00000679967.1:c.2356G>C	ENSP00000506607.1:p.Gly786Arg
ENST00000680327.1:c.*1398G>C	ENSP00000506639.1:n.*1398G>C
ENST00000680448.1:c.2356G>C	ENSP00000505921.1:p.Gly786Arg
ENST00000680657.1:n.2467G>C
ENST00000680690.1:c.*1608G>C	ENSP00000506121.1:n.*1608G>C
ENST00000680888.1:c.2356G>C	ENSP00000506276.1:p.Gly786Arg
ENST00000680947.1:c.*1628G>C	ENSP00000506496.1:n.*1628G>C
ENST00000681024.1:c.2356G>C	ENSP00000506449.1:p.Gly786Arg
ENST00000681083.1:c.*2090G>C	ENSP00000506095.1:n.*2090G>C
ENST00000681167.1:n.2230G>C
ENST00000681483.1:c.2356G>C	ENSP00000505499.1:p.Gly786Arg
ENST00000681502.1:c.*1780G>C	ENSP00000505644.1:n.*1780G>C
ENST00000681606.1:c.2356G>C	ENSP00000505354.1:p.Gly786Arg
ENST00000681819.1:c.2356G>C	ENSP00000505673.1:p.Gly786Arg
ENST00000681952.1:c.2356G>C	ENSP00000506400.1:p.Gly786Arg
XM_006712761.1:c.2356G>C	XP_006712824.1:p.Gly786Arg
XM_011511870.1:c.1789G>C	XP_011510172.1:p.Gly597Arg
XM_011511871.1:c.1606G>C	XP_011510173.1:p.Gly536Arg
XM_011511871.3:c.1606G>C	XP_011510173.1:p.Gly536Arg
XM_011511872.1:c.2356G>C	XP_011510174.1:p.Gly786Arg
XM_011511872.2:c.2356G>C	XP_011510174.1:p.Gly786Arg
XM_017004967.1:c.2356G>C	XP_016860456.1:p.Gly786Arg
XM_017004968.2:c.1702G>C	XP_016860457.1:p.Gly568Arg
XM_017004969.1:c.1357G>C	XP_016860458.1:p.Gly453Arg