Canonical Allele Identifier: CA1941650

Gene: TTC21B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165898670A>G , CM000664.2:g.165898670A>G	GRCh38
NC_000002.11:g.166755180A>G , CM000664.1:g.166755180A>G	GRCh37
NC_000002.10:g.166463426A>G	NCBI36
NG_030345.1:g.60169T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000243344.8:c.2950+16T>C MANE Select	ENSP00000243344.7:n.2950+16T>C
ENST00000652557.1:c.2950+16T>C	ENSP00000498617.1:n.2950+16T>C
ENST00000679356.1:c.2950+16T>C	ENSP00000506245.1:n.2950+16T>C
ENST00000679676.1:c.2839+16T>C	ENSP00000505492.1:n.2839+16T>C
ENST00000679799.1:c.2950+16T>C	ENSP00000505208.1:n.2950+16T>C
ENST00000679840.1:c.2950+16T>C	ENSP00000505248.1:n.2950+16T>C
ENST00000679931.1:c.*1992+16T>C	ENSP00000505632.1:n.*1992+16T>C
ENST00000679967.1:c.2941+25T>C	ENSP00000506607.1:n.2941+25T>C
ENST00000680327.1:c.*1992+16T>C	ENSP00000506639.1:n.*1992+16T>C
ENST00000680448.1:c.2950+16T>C	ENSP00000505921.1:n.2950+16T>C
ENST00000680657.1:n.3061+16T>C
ENST00000680690.1:c.*2202+16T>C	ENSP00000506121.1:n.*2202+16T>C
ENST00000680888.1:c.2950+16T>C	ENSP00000506276.1:n.2950+16T>C
ENST00000680925.1:n.980+16T>C
ENST00000680947.1:c.*2222+16T>C	ENSP00000506496.1:n.*2222+16T>C
ENST00000681024.1:c.2950+16T>C	ENSP00000506449.1:n.2950+16T>C
ENST00000681083.1:c.*2684+16T>C	ENSP00000506095.1:n.*2684+16T>C
ENST00000681167.1:n.2824+16T>C
ENST00000681483.1:c.2950+16T>C	ENSP00000505499.1:n.2950+16T>C
ENST00000681502.1:c.*2374+16T>C	ENSP00000505644.1:n.*2374+16T>C
ENST00000681606.1:c.2950+16T>C	ENSP00000505354.1:n.2950+16T>C
ENST00000681819.1:c.2950+16T>C	ENSP00000505673.1:n.2950+16T>C
ENST00000681952.1:c.2950+16T>C	ENSP00000506400.1:n.2950+16T>C
ENST00000243344.7:c.2950+16T>C	ENSP00000243344.7:n.2950+16T>C
ENST00000484129.1:n.441T>C
NM_024753.4:c.2950+16T>C	NP_079029.3:n.2950+16T>C
XM_006712761.1:c.2950+16T>C	XP_006712824.1:n.2950+16T>C
XM_011511870.1:c.2383+16T>C	XP_011510172.1:n.2383+16T>C
XM_011511871.1:c.2200+16T>C	XP_011510173.1:n.2200+16T>C
XM_011511872.1:c.*152+16T>C	XP_011510174.1:n.*152+16T>C
XM_011511871.3:c.2200+16T>C	XP_011510173.1:n.2200+16T>C
XM_011511872.2:c.*152+16T>C	XP_011510174.1:n.*152+16T>C
XM_017004967.1:c.2950+16T>C	XP_016860456.1:n.2950+16T>C
XM_017004968.2:c.2296+16T>C	XP_016860457.1:n.2296+16T>C
XM_017004969.1:c.1951+16T>C	XP_016860458.1:n.1951+16T>C
NM_024753.5:c.2950+16T>C MANE Select	NP_079029.3:n.2950+16T>C