Canonical Allele Identifier: CA1941451

Gene: TTC21B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165883793C>T , CM000664.2:g.165883793C>T	GRCh38
NC_000002.11:g.166740303C>T , CM000664.1:g.166740303C>T	GRCh37
NC_000002.10:g.166448549C>T	NCBI36
NG_030345.1:g.75046G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_024753.5:c.3684+1G>A MANE Select	NP_079029.3:n.3684+1G>A
ENST00000243344.8:c.3684+1G>A MANE Select	ENSP00000243344.7:n.3684+1G>A
NM_024753.4:c.3684+1G>A	NP_079029.3:n.3684+1G>A
ENST00000243344.7:c.3684+1G>A	ENSP00000243344.7:n.3684+1G>A
ENST00000392695.6:c.584+1G>A
ENST00000497425.1:n.162+1G>A
ENST00000497425.2:n.793+1G>A
ENST00000652557.1:c.3684+1G>A	ENSP00000498617.1:n.3684+1G>A
ENST00000679356.1:c.3681+1G>A	ENSP00000506245.1:n.3681+1G>A
ENST00000679676.1:c.3573+1G>A	ENSP00000505492.1:n.3573+1G>A
ENST00000679799.1:c.3684+1G>A	ENSP00000505208.1:n.3684+1G>A
ENST00000679840.1:c.3684+1G>A	ENSP00000505248.1:n.3684+1G>A
ENST00000679931.1:c.*2726+1G>A	ENSP00000505632.1:n.*2726+1G>A
ENST00000679967.1:c.3675+1G>A	ENSP00000506607.1:n.3675+1G>A
ENST00000680327.1:c.*2726+1G>A	ENSP00000506639.1:n.*2726+1G>A
ENST00000680657.1:n.3795+1G>A
ENST00000680690.1:c.*2936+1G>A	ENSP00000506121.1:n.*2936+1G>A
ENST00000680888.1:c.3684+1G>A	ENSP00000506276.1:n.3684+1G>A
ENST00000680925.1:n.1714+1G>A
ENST00000680947.1:c.*2956+1G>A	ENSP00000506496.1:n.*2956+1G>A
ENST00000681024.1:c.3684+1G>A	ENSP00000506449.1:n.3684+1G>A
ENST00000681083.1:c.*3415+1G>A	ENSP00000506095.1:n.*3415+1G>A
ENST00000681167.1:n.3559G>A
ENST00000681483.1:c.*494+1G>A	ENSP00000505499.1:n.*494+1G>A
ENST00000681502.1:c.*6944+1G>A	ENSP00000505644.1:n.*6944+1G>A
ENST00000681819.1:c.*494+1G>A	ENSP00000505673.1:n.*494+1G>A
ENST00000681952.1:c.3684+1G>A	ENSP00000506400.1:n.3684+1G>A
XM_011511870.1:c.3117+1G>A	XP_011510172.1:n.3117+1G>A
XM_011511871.1:c.2934+1G>A	XP_011510173.1:n.2934+1G>A
XM_011511871.3:c.2934+1G>A	XP_011510173.1:n.2934+1G>A
XM_011511872.2:c.*886+1G>A	XP_011510174.1:n.*886+1G>A
XM_017004967.1:c.3684+1G>A	XP_016860456.1:n.3684+1G>A
XM_017004968.2:c.3030+1G>A	XP_016860457.1:n.3030+1G>A
XM_017004969.1:c.2685+1G>A	XP_016860458.1:n.2685+1G>A