Canonical Allele Identifier: CA1942250

Gene: TTC21B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165930171C>T , CM000664.2:g.165930171C>T	GRCh38
NC_000002.11:g.166786681C>T , CM000664.1:g.166786681C>T	GRCh37
NC_000002.10:g.166494927C>T	NCBI36
NG_030345.1:g.28668G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_024753.5:c.1087+1G>A MANE Select	NP_079029.3:n.1087+1G>A
ENST00000243344.8:c.1087+1G>A MANE Select	ENSP00000243344.7:n.1087+1G>A
NM_024753.4:c.1087+1G>A	NP_079029.3:n.1087+1G>A
ENST00000243344.7:c.1087+1G>A	ENSP00000243344.7:n.1087+1G>A
ENST00000464374.5:n.1127+1G>A
ENST00000652557.1:c.1087+1G>A	ENSP00000498617.1:n.1087+1G>A
ENST00000679356.1:c.1087+1G>A	ENSP00000506245.1:n.1087+1G>A
ENST00000679671.1:n.1200+1G>A
ENST00000679676.1:c.976+1G>A	ENSP00000505492.1:n.976+1G>A
ENST00000679799.1:c.1087+1G>A	ENSP00000505208.1:n.1087+1G>A
ENST00000679840.1:c.1087+1G>A	ENSP00000505248.1:n.1087+1G>A
ENST00000679931.1:c.*129+1G>A	ENSP00000505632.1:n.*129+1G>A
ENST00000679967.1:c.1087+1G>A	ENSP00000506607.1:n.1087+1G>A
ENST00000680225.1:n.346+1G>A
ENST00000680327.1:c.*129+1G>A	ENSP00000506639.1:n.*129+1G>A
ENST00000680448.1:c.1087+1G>A	ENSP00000505921.1:n.1087+1G>A
ENST00000680657.1:n.1198+1G>A
ENST00000680690.1:c.*339+1G>A	ENSP00000506121.1:n.*339+1G>A
ENST00000680888.1:c.1087+1G>A	ENSP00000506276.1:n.1087+1G>A
ENST00000680947.1:c.*359+1G>A	ENSP00000506496.1:n.*359+1G>A
ENST00000681024.1:c.1087+1G>A	ENSP00000506449.1:n.1087+1G>A
ENST00000681083.1:c.*821+1G>A	ENSP00000506095.1:n.*821+1G>A
ENST00000681167.1:n.961+1G>A
ENST00000681483.1:c.1087+1G>A	ENSP00000505499.1:n.1087+1G>A
ENST00000681502.1:c.*511+1G>A	ENSP00000505644.1:n.*511+1G>A
ENST00000681606.1:c.1087+1G>A	ENSP00000505354.1:n.1087+1G>A
ENST00000681819.1:c.1087+1G>A	ENSP00000505673.1:n.1087+1G>A
ENST00000681952.1:c.1087+1G>A	ENSP00000506400.1:n.1087+1G>A
XM_006712761.1:c.1087+1G>A	XP_006712824.1:n.1087+1G>A
XM_011511870.1:c.520+1G>A	XP_011510172.1:n.520+1G>A
XM_011511871.1:c.337+1G>A	XP_011510173.1:n.337+1G>A
XM_011511871.3:c.337+1G>A	XP_011510173.1:n.337+1G>A
XM_011511872.1:c.1087+1G>A	XP_011510174.1:n.1087+1G>A
XM_011511872.2:c.1087+1G>A	XP_011510174.1:n.1087+1G>A
XM_017004967.1:c.1087+1G>A	XP_016860456.1:n.1087+1G>A
XM_017004968.2:c.433+1G>A	XP_016860457.1:n.433+1G>A
XM_017004969.1:c.88+1G>A	XP_016860458.1:n.88+1G>A