Canonical Allele Identifier: CA1942083
Community Standard Title: NM_024753.5(TTC21B):c.1563C>T (p.His521=)
Gene: TTC21B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.165919387G>A , CM000664.2:g.165919387G>A GRCh38
NC_000002.11:g.166775897G>A , CM000664.1:g.166775897G>A GRCh37
NC_000002.10:g.166484143G>A NCBI36
NG_030345.1:g.39452C>T

Transcript Alleles

HGVS Amino-acid Change
NM_024753.5:c.1563C>T MANE Select NP_079029.3:p.His521=
ENST00000243344.8:c.1563C>T MANE Select ENSP00000243344.7:p.His521=
NM_024753.4:c.1563C>T NP_079029.3:p.His521=
ENST00000243344.7:c.1563C>T ENSP00000243344.7:p.His521=
ENST00000652557.1:c.1563C>T ENSP00000498617.1:p.His521=
ENST00000679356.1:c.1563C>T ENSP00000506245.1:p.His521=
ENST00000679671.1:n.1676C>T
ENST00000679676.1:c.1452C>T ENSP00000505492.1:p.His484=
ENST00000679799.1:c.1563C>T ENSP00000505208.1:p.His521=
ENST00000679840.1:c.1563C>T ENSP00000505248.1:p.His521=
ENST00000679931.1:c.*605C>T ENSP00000505632.1:n.*605C>T
ENST00000679967.1:c.1563C>T ENSP00000506607.1:p.His521=
ENST00000680327.1:c.*605C>T ENSP00000506639.1:n.*605C>T
ENST00000680448.1:c.1563C>T ENSP00000505921.1:p.His521=
ENST00000680657.1:n.1674C>T
ENST00000680690.1:c.*815C>T ENSP00000506121.1:n.*815C>T
ENST00000680888.1:c.1563C>T ENSP00000506276.1:p.His521=
ENST00000680947.1:c.*835C>T ENSP00000506496.1:n.*835C>T
ENST00000681024.1:c.1563C>T ENSP00000506449.1:p.His521=
ENST00000681083.1:c.*1297C>T ENSP00000506095.1:n.*1297C>T
ENST00000681167.1:n.1437C>T
ENST00000681483.1:c.1563C>T ENSP00000505499.1:p.His521=
ENST00000681502.1:c.*987C>T ENSP00000505644.1:n.*987C>T
ENST00000681606.1:c.1563C>T ENSP00000505354.1:p.His521=
ENST00000681819.1:c.1563C>T ENSP00000505673.1:p.His521=
ENST00000681952.1:c.1563C>T ENSP00000506400.1:p.His521=
XM_006712761.1:c.1563C>T XP_006712824.1:p.His521=
XM_011511870.1:c.996C>T XP_011510172.1:p.His332=
XM_011511871.1:c.813C>T XP_011510173.1:p.His271=
XM_011511871.3:c.813C>T XP_011510173.1:p.His271=
XM_011511872.1:c.1563C>T XP_011510174.1:p.His521=
XM_011511872.2:c.1563C>T XP_011510174.1:p.His521=
XM_017004967.1:c.1563C>T XP_016860456.1:p.His521=
XM_017004968.2:c.909C>T XP_016860457.1:p.His303=
XM_017004969.1:c.564C>T XP_016860458.1:p.His188=