Canonical Allele Identifier: CA349056856
Community Standard Title: NM_024753.5(TTC21B):c.2461+1G>A
Gene: TTC21B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.165911326C>T , CM000664.2:g.165911326C>T GRCh38
NC_000002.11:g.166767836C>T , CM000664.1:g.166767836C>T GRCh37
NC_000002.10:g.166476082C>T NCBI36
NG_030345.1:g.47513G>A

Transcript Alleles

HGVS Amino-acid Change
NM_024753.5:c.2461+1G>A MANE Select NP_079029.3:n.2461+1G>A
ENST00000243344.8:c.2461+1G>A MANE Select ENSP00000243344.7:n.2461+1G>A
NM_024753.4:c.2461+1G>A NP_079029.3:n.2461+1G>A
ENST00000243344.7:c.2461+1G>A ENSP00000243344.7:n.2461+1G>A
ENST00000652557.1:c.2461+1G>A ENSP00000498617.1:n.2461+1G>A
ENST00000679356.1:c.2461+1G>A ENSP00000506245.1:n.2461+1G>A
ENST00000679671.1:n.2575G>A
ENST00000679676.1:c.2350+1G>A ENSP00000505492.1:n.2350+1G>A
ENST00000679799.1:c.2461+1G>A ENSP00000505208.1:n.2461+1G>A
ENST00000679840.1:c.2461+1G>A ENSP00000505248.1:n.2461+1G>A
ENST00000679931.1:c.*1503+1G>A ENSP00000505632.1:n.*1503+1G>A
ENST00000679967.1:c.2461+1G>A ENSP00000506607.1:n.2461+1G>A
ENST00000680327.1:c.*1503+1G>A ENSP00000506639.1:n.*1503+1G>A
ENST00000680448.1:c.2461+1G>A ENSP00000505921.1:n.2461+1G>A
ENST00000680657.1:n.2572+1G>A
ENST00000680690.1:c.*1713+1G>A ENSP00000506121.1:n.*1713+1G>A
ENST00000680888.1:c.2461+1G>A ENSP00000506276.1:n.2461+1G>A
ENST00000680947.1:c.*1733+1G>A ENSP00000506496.1:n.*1733+1G>A
ENST00000681024.1:c.2461+1G>A ENSP00000506449.1:n.2461+1G>A
ENST00000681083.1:c.*2195+1G>A ENSP00000506095.1:n.*2195+1G>A
ENST00000681167.1:n.2335+1G>A
ENST00000681483.1:c.2461+1G>A ENSP00000505499.1:n.2461+1G>A
ENST00000681502.1:c.*1885+1G>A ENSP00000505644.1:n.*1885+1G>A
ENST00000681606.1:c.2461+1G>A ENSP00000505354.1:n.2461+1G>A
ENST00000681819.1:c.2461+1G>A ENSP00000505673.1:n.2461+1G>A
ENST00000681952.1:c.2461+1G>A ENSP00000506400.1:n.2461+1G>A
XM_006712761.1:c.2461+1G>A XP_006712824.1:n.2461+1G>A
XM_011511870.1:c.1894+1G>A XP_011510172.1:n.1894+1G>A
XM_011511871.1:c.1711+1G>A XP_011510173.1:n.1711+1G>A
XM_011511871.3:c.1711+1G>A XP_011510173.1:n.1711+1G>A
XM_011511872.1:c.2461+1G>A XP_011510174.1:n.2461+1G>A
XM_011511872.2:c.2461+1G>A XP_011510174.1:n.2461+1G>A
XM_017004967.1:c.2461+1G>A XP_016860456.1:n.2461+1G>A
XM_017004968.2:c.1807+1G>A XP_016860457.1:n.1807+1G>A
XM_017004969.1:c.1462+1G>A XP_016860458.1:n.1462+1G>A