Canonical Allele Identifier: CA1941512

Gene: TTC21B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165888288T>C , CM000664.2:g.165888288T>C	GRCh38
NC_000002.11:g.166744798T>C , CM000664.1:g.166744798T>C	GRCh37
NC_000002.10:g.166453044T>C	NCBI36
NG_030345.1:g.70551A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_024753.5:c.3450A>G MANE Select	NP_079029.3:p.Ala1150=
ENST00000243344.8:c.3450A>G MANE Select	ENSP00000243344.7:p.Ala1150=
NM_024753.4:c.3450A>G	NP_079029.3:p.Ala1150=
ENST00000243344.7:c.3450A>G	ENSP00000243344.7:p.Ala1150=
ENST00000392695.6:c.350A>G
ENST00000652557.1:c.3450A>G	ENSP00000498617.1:p.Ala1150=
ENST00000679356.1:c.3450A>G	ENSP00000506245.1:p.Ala1150=
ENST00000679676.1:c.3339A>G	ENSP00000505492.1:p.Ala1113=
ENST00000679799.1:c.3450A>G	ENSP00000505208.1:p.Ala1150=
ENST00000679840.1:c.3450A>G	ENSP00000505248.1:p.Ala1150=
ENST00000679931.1:c.*2492A>G	ENSP00000505632.1:n.*2492A>G
ENST00000679967.1:c.3441A>G	ENSP00000506607.1:p.Ala1147=
ENST00000680327.1:c.*2492A>G	ENSP00000506639.1:n.*2492A>G
ENST00000680657.1:n.3561A>G
ENST00000680690.1:c.*2702A>G	ENSP00000506121.1:n.*2702A>G
ENST00000680888.1:c.3450A>G	ENSP00000506276.1:p.Ala1150=
ENST00000680925.1:n.1480A>G
ENST00000680947.1:c.*2722A>G	ENSP00000506496.1:n.*2722A>G
ENST00000681024.1:c.3450A>G	ENSP00000506449.1:p.Ala1150=
ENST00000681083.1:c.*3184A>G	ENSP00000506095.1:n.*3184A>G
ENST00000681167.1:n.3324A>G
ENST00000681483.1:c.*260A>G	ENSP00000505499.1:n.*260A>G
ENST00000681502.1:c.*6710A>G	ENSP00000505644.1:n.*6710A>G
ENST00000681819.1:c.*260A>G	ENSP00000505673.1:n.*260A>G
ENST00000681952.1:c.3450A>G	ENSP00000506400.1:p.Ala1150=
XM_011511870.1:c.2883A>G	XP_011510172.1:p.Ala961=
XM_011511871.1:c.2700A>G	XP_011510173.1:p.Ala900=
XM_011511871.3:c.2700A>G	XP_011510173.1:p.Ala900=
XM_011511872.2:c.*652A>G	XP_011510174.1:n.*652A>G
XM_017004967.1:c.3450A>G	XP_016860456.1:p.Ala1150=
XM_017004968.2:c.2796A>G	XP_016860457.1:p.Ala932=
XM_017004969.1:c.2451A>G	XP_016860458.1:p.Ala817=