Canonical Allele Identifier: CA1941462
Community Standard Title: NM_024753.5(TTC21B):c.3631G>A (p.Ala1211Thr)
Gene: TTC21B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.165883847C>T , CM000664.2:g.165883847C>T GRCh38
NC_000002.11:g.166740357C>T , CM000664.1:g.166740357C>T GRCh37
NC_000002.10:g.166448603C>T NCBI36
NG_030345.1:g.74992G>A

Transcript Alleles

HGVS Amino-acid Change
NM_024753.5:c.3631G>A MANE Select NP_079029.3:p.Ala1211Thr
ENST00000243344.8:c.3631G>A MANE Select ENSP00000243344.7:p.Ala1211Thr
NM_024753.4:c.3631G>A NP_079029.3:p.Ala1211Thr
ENST00000243344.7:c.3631G>A ENSP00000243344.7:p.Ala1211Thr
ENST00000392695.6:c.531G>A
ENST00000497425.1:n.109G>A
ENST00000497425.2:n.740G>A
ENST00000652557.1:c.3631G>A ENSP00000498617.1:p.Ala1211Thr
ENST00000679356.1:c.3628G>A ENSP00000506245.1:p.Ala1210Thr
ENST00000679676.1:c.3520G>A ENSP00000505492.1:p.Ala1174Thr
ENST00000679799.1:c.3631G>A ENSP00000505208.1:p.Ala1211Thr
ENST00000679840.1:c.3631G>A ENSP00000505248.1:p.Ala1211Thr
ENST00000679931.1:c.*2673G>A ENSP00000505632.1:n.*2673G>A
ENST00000679967.1:c.3622G>A ENSP00000506607.1:p.Ala1208Thr
ENST00000680327.1:c.*2673G>A ENSP00000506639.1:n.*2673G>A
ENST00000680657.1:n.3742G>A
ENST00000680690.1:c.*2883G>A ENSP00000506121.1:n.*2883G>A
ENST00000680888.1:c.3631G>A ENSP00000506276.1:p.Ala1211Thr
ENST00000680925.1:n.1661G>A
ENST00000680947.1:c.*2903G>A ENSP00000506496.1:n.*2903G>A
ENST00000681024.1:c.3631G>A ENSP00000506449.1:p.Ala1211Thr
ENST00000681083.1:c.*3362G>A ENSP00000506095.1:n.*3362G>A
ENST00000681167.1:n.3505G>A
ENST00000681483.1:c.*441G>A ENSP00000505499.1:n.*441G>A
ENST00000681502.1:c.*6891G>A ENSP00000505644.1:n.*6891G>A
ENST00000681819.1:c.*441G>A ENSP00000505673.1:n.*441G>A
ENST00000681952.1:c.3631G>A ENSP00000506400.1:p.Ala1211Thr
XM_011511870.1:c.3064G>A XP_011510172.1:p.Ala1022Thr
XM_011511871.1:c.2881G>A XP_011510173.1:p.Ala961Thr
XM_011511871.3:c.2881G>A XP_011510173.1:p.Ala961Thr
XM_011511872.2:c.*833G>A XP_011510174.1:n.*833G>A
XM_017004967.1:c.3631G>A XP_016860456.1:p.Ala1211Thr
XM_017004968.2:c.2977G>A XP_016860457.1:p.Ala993Thr
XM_017004969.1:c.2632G>A XP_016860458.1:p.Ala878Thr