Canonical Allele Identifier: CA1942163

Gene: TTC21B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165929134C>A , CM000664.2:g.165929134C>A	GRCh38
NC_000002.11:g.166785644C>A , CM000664.1:g.166785644C>A	GRCh37
NC_000002.10:g.166493890C>A	NCBI36
NG_030345.1:g.29705G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_024753.5:c.1386+1G>T MANE Select	NP_079029.3:n.1386+1G>T
ENST00000243344.8:c.1386+1G>T MANE Select	ENSP00000243344.7:n.1386+1G>T
NM_024753.4:c.1386+1G>T	NP_079029.3:n.1386+1G>T
ENST00000243344.7:c.1386+1G>T	ENSP00000243344.7:n.1386+1G>T
ENST00000464374.5:n.1427G>T
ENST00000652557.1:c.1386+1G>T	ENSP00000498617.1:n.1386+1G>T
ENST00000679356.1:c.1386+1G>T	ENSP00000506245.1:n.1386+1G>T
ENST00000679671.1:n.1499+1G>T
ENST00000679676.1:c.1275+1G>T	ENSP00000505492.1:n.1275+1G>T
ENST00000679799.1:c.1386+1G>T	ENSP00000505208.1:n.1386+1G>T
ENST00000679840.1:c.1386+1G>T	ENSP00000505248.1:n.1386+1G>T
ENST00000679931.1:c.*428+1G>T	ENSP00000505632.1:n.*428+1G>T
ENST00000679967.1:c.1386+1G>T	ENSP00000506607.1:n.1386+1G>T
ENST00000680225.1:n.645+1G>T
ENST00000680327.1:c.*428+1G>T	ENSP00000506639.1:n.*428+1G>T
ENST00000680448.1:c.1386+1G>T	ENSP00000505921.1:n.1386+1G>T
ENST00000680657.1:n.1497+1G>T
ENST00000680690.1:c.*638+1G>T	ENSP00000506121.1:n.*638+1G>T
ENST00000680888.1:c.1386+1G>T	ENSP00000506276.1:n.1386+1G>T
ENST00000680947.1:c.*658+1G>T	ENSP00000506496.1:n.*658+1G>T
ENST00000681024.1:c.1386+1G>T	ENSP00000506449.1:n.1386+1G>T
ENST00000681083.1:c.*1120+1G>T	ENSP00000506095.1:n.*1120+1G>T
ENST00000681167.1:n.1260+1G>T
ENST00000681483.1:c.1386+1G>T	ENSP00000505499.1:n.1386+1G>T
ENST00000681502.1:c.*810+1G>T	ENSP00000505644.1:n.*810+1G>T
ENST00000681606.1:c.1386+1G>T	ENSP00000505354.1:n.1386+1G>T
ENST00000681819.1:c.1386+1G>T	ENSP00000505673.1:n.1386+1G>T
ENST00000681952.1:c.1386+1G>T	ENSP00000506400.1:n.1386+1G>T
XM_006712761.1:c.1386+1G>T	XP_006712824.1:n.1386+1G>T
XM_011511870.1:c.819+1G>T	XP_011510172.1:n.819+1G>T
XM_011511871.1:c.636+1G>T	XP_011510173.1:n.636+1G>T
XM_011511871.3:c.636+1G>T	XP_011510173.1:n.636+1G>T
XM_011511872.1:c.1386+1G>T	XP_011510174.1:n.1386+1G>T
XM_011511872.2:c.1386+1G>T	XP_011510174.1:n.1386+1G>T
XM_017004967.1:c.1386+1G>T	XP_016860456.1:n.1386+1G>T
XM_017004968.2:c.732+1G>T	XP_016860457.1:n.732+1G>T
XM_017004969.1:c.387+1G>T	XP_016860458.1:n.387+1G>T