Canonical Allele Identifier: CA1941774

Gene: TTC21B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165901910C>T , CM000664.2:g.165901910C>T	GRCh38
NC_000002.11:g.166758420C>T , CM000664.1:g.166758420C>T	GRCh37
NC_000002.10:g.166466666C>T	NCBI36
NG_030345.1:g.56929G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_024753.5:c.2569G>A MANE Select	NP_079029.3:p.Ala857Thr
ENST00000243344.8:c.2569G>A MANE Select	ENSP00000243344.7:p.Ala857Thr
NM_024753.4:c.2569G>A	NP_079029.3:p.Ala857Thr
ENST00000243344.7:c.2569G>A	ENSP00000243344.7:p.Ala857Thr
ENST00000484129.1:n.44G>A
ENST00000652557.1:c.2569G>A	ENSP00000498617.1:p.Ala857Thr
ENST00000679356.1:c.2569G>A	ENSP00000506245.1:p.Ala857Thr
ENST00000679676.1:c.2458G>A	ENSP00000505492.1:p.Ala820Thr
ENST00000679799.1:c.2569G>A	ENSP00000505208.1:p.Ala857Thr
ENST00000679840.1:c.2569G>A	ENSP00000505248.1:p.Ala857Thr
ENST00000679931.1:c.*1611G>A	ENSP00000505632.1:n.*1611G>A
ENST00000679967.1:c.2569G>A	ENSP00000506607.1:p.Ala857Thr
ENST00000680327.1:c.*1611G>A	ENSP00000506639.1:n.*1611G>A
ENST00000680448.1:c.2569G>A	ENSP00000505921.1:p.Ala857Thr
ENST00000680657.1:n.2680G>A
ENST00000680690.1:c.*1821G>A	ENSP00000506121.1:n.*1821G>A
ENST00000680888.1:c.2569G>A	ENSP00000506276.1:p.Ala857Thr
ENST00000680925.1:n.568G>A
ENST00000680947.1:c.*1841G>A	ENSP00000506496.1:n.*1841G>A
ENST00000681024.1:c.2569G>A	ENSP00000506449.1:p.Ala857Thr
ENST00000681083.1:c.*2303G>A	ENSP00000506095.1:n.*2303G>A
ENST00000681167.1:n.2443G>A
ENST00000681483.1:c.2569G>A	ENSP00000505499.1:p.Ala857Thr
ENST00000681502.1:c.*1993G>A	ENSP00000505644.1:n.*1993G>A
ENST00000681606.1:c.2569G>A	ENSP00000505354.1:p.Ala857Thr
ENST00000681819.1:c.2569G>A	ENSP00000505673.1:p.Ala857Thr
ENST00000681952.1:c.2569G>A	ENSP00000506400.1:p.Ala857Thr
XM_006712761.1:c.2569G>A	XP_006712824.1:p.Ala857Thr
XM_011511870.1:c.2002G>A	XP_011510172.1:p.Ala668Thr
XM_011511871.1:c.1819G>A	XP_011510173.1:p.Ala607Thr
XM_011511871.3:c.1819G>A	XP_011510173.1:p.Ala607Thr
XM_011511872.1:c.2569G>A	XP_011510174.1:p.Ala857Thr
XM_011511872.2:c.2569G>A	XP_011510174.1:p.Ala857Thr
XM_017004967.1:c.2569G>A	XP_016860456.1:p.Ala857Thr
XM_017004968.2:c.1915G>A	XP_016860457.1:p.Ala639Thr
XM_017004969.1:c.1570G>A	XP_016860458.1:p.Ala524Thr