Canonical Allele Identifier: CA349127

Gene: TTC21B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165912511T>C , CM000664.2:g.165912511T>C	GRCh38
NC_000002.11:g.166769021T>C , CM000664.1:g.166769021T>C	GRCh37
NC_000002.10:g.166477267T>C	NCBI36
NG_030345.1:g.46328A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000243344.8:c.2322+3A>G MANE Select	ENSP00000243344.7:n.2322+3A>G
ENST00000652557.1:c.2322+3A>G	ENSP00000498617.1:n.2322+3A>G
ENST00000679356.1:c.2322+3A>G	ENSP00000506245.1:n.2322+3A>G
ENST00000679671.1:n.2435+3A>G
ENST00000679676.1:c.2211+3A>G	ENSP00000505492.1:n.2211+3A>G
ENST00000679799.1:c.2322+3A>G	ENSP00000505208.1:n.2322+3A>G
ENST00000679840.1:c.2322+3A>G	ENSP00000505248.1:n.2322+3A>G
ENST00000679931.1:c.*1364+3A>G	ENSP00000505632.1:n.*1364+3A>G
ENST00000679967.1:c.2322+3A>G	ENSP00000506607.1:n.2322+3A>G
ENST00000680327.1:c.*1364+3A>G	ENSP00000506639.1:n.*1364+3A>G
ENST00000680448.1:c.2322+3A>G	ENSP00000505921.1:n.2322+3A>G
ENST00000680657.1:n.2433+3A>G
ENST00000680690.1:c.*1574+3A>G	ENSP00000506121.1:n.*1574+3A>G
ENST00000680888.1:c.2322+3A>G	ENSP00000506276.1:n.2322+3A>G
ENST00000680947.1:c.*1594+3A>G	ENSP00000506496.1:n.*1594+3A>G
ENST00000681024.1:c.2322+3A>G	ENSP00000506449.1:n.2322+3A>G
ENST00000681083.1:c.*2056+3A>G	ENSP00000506095.1:n.*2056+3A>G
ENST00000681167.1:n.2196+3A>G
ENST00000681483.1:c.2322+3A>G	ENSP00000505499.1:n.2322+3A>G
ENST00000681502.1:c.*1746+3A>G	ENSP00000505644.1:n.*1746+3A>G
ENST00000681606.1:c.2322+3A>G	ENSP00000505354.1:n.2322+3A>G
ENST00000681819.1:c.2322+3A>G	ENSP00000505673.1:n.2322+3A>G
ENST00000681952.1:c.2322+3A>G	ENSP00000506400.1:n.2322+3A>G
ENST00000243344.7:c.2322+3A>G	ENSP00000243344.7:n.2322+3A>G
NM_024753.4:c.2322+3A>G	NP_079029.3:n.2322+3A>G
XM_006712761.1:c.2322+3A>G	XP_006712824.1:n.2322+3A>G
XM_011511870.1:c.1755+3A>G	XP_011510172.1:n.1755+3A>G
XM_011511871.1:c.1572+3A>G	XP_011510173.1:n.1572+3A>G
XM_011511872.1:c.2322+3A>G	XP_011510174.1:n.2322+3A>G
XM_011511871.3:c.1572+3A>G	XP_011510173.1:n.1572+3A>G
XM_011511872.2:c.2322+3A>G	XP_011510174.1:n.2322+3A>G
XM_017004967.1:c.2322+3A>G	XP_016860456.1:n.2322+3A>G
XM_017004968.2:c.1668+3A>G	XP_016860457.1:n.1668+3A>G
XM_017004969.1:c.1323+3A>G	XP_016860458.1:n.1323+3A>G
NM_024753.5:c.2322+3A>G MANE Select	NP_079029.3:n.2322+3A>G