Canonical Allele Identifier: CA10612723

Gene: TTC21B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165874650C>T , CM000664.2:g.165874650C>T	GRCh38
NC_000002.11:g.166731160C>T , CM000664.1:g.166731160C>T	GRCh37
NC_000002.10:g.166439406C>T	NCBI36
NG_030345.1:g.84189G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000243344.8:c.*105G>A MANE Select	ENSP00000243344.7:n.*105G>A
ENST00000652557.1:c.3806-3630G>A	ENSP00000498617.1:n.3806-3630G>A
ENST00000679356.1:c.*105G>A	ENSP00000506245.1:n.*105G>A
ENST00000679676.1:c.*105G>A	ENSP00000505492.1:n.*105G>A
ENST00000679799.1:c.3806-3630G>A	ENSP00000505208.1:n.3806-3630G>A
ENST00000679931.1:c.*3069+29G>A	ENSP00000505632.1:n.*3069+29G>A
ENST00000679967.1:c.*105G>A	ENSP00000506607.1:n.*105G>A
ENST00000680327.1:c.*3098G>A	ENSP00000506639.1:n.*3098G>A
ENST00000680657.1:n.5499G>A
ENST00000680690.1:c.*3308G>A	ENSP00000506121.1:n.*3308G>A
ENST00000680888.1:c.*105G>A	ENSP00000506276.1:n.*105G>A
ENST00000680904.1:n.560G>A
ENST00000680947.1:c.*3328G>A	ENSP00000506496.1:n.*3328G>A
ENST00000681024.1:c.*3846G>A	ENSP00000506449.1:n.*3846G>A
ENST00000681083.1:c.*3787G>A	ENSP00000506095.1:n.*3787G>A
ENST00000681167.1:n.3934G>A
ENST00000681483.1:c.*837+29G>A	ENSP00000505499.1:n.*837+29G>A
ENST00000681502.1:c.*7316G>A	ENSP00000505644.1:n.*7316G>A
ENST00000681819.1:c.*866G>A	ENSP00000505673.1:n.*866G>A
ENST00000681952.1:c.*76+29G>A	ENSP00000506400.1:n.*76+29G>A
ENST00000243344.7:c.*105G>A	ENSP00000243344.7:n.*105G>A
ENST00000392695.6:c.927+29G>A
NM_024753.4:c.*105G>A	NP_079029.3:n.*105G>A
XM_011511870.1:c.*105G>A	XP_011510172.1:n.*105G>A
XM_011511871.1:c.*105G>A	XP_011510173.1:n.*105G>A
XM_011511871.3:c.*105G>A	XP_011510173.1:n.*105G>A
XM_011511872.2:c.*1258G>A	XP_011510174.1:n.*1258G>A
XM_017004968.2:c.*105G>A	XP_016860457.1:n.*105G>A
XM_017004969.1:c.*105G>A	XP_016860458.1:n.*105G>A
NM_024753.5:c.*105G>A MANE Select	NP_079029.3:n.*105G>A