Canonical Allele Identifier: CA155842

Gene: TTC21B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165924678G>A , CM000664.2:g.165924678G>A	GRCh38
NC_000002.11:g.166781188G>A , CM000664.1:g.166781188G>A	GRCh37
NC_000002.10:g.166489434G>A	NCBI36
NG_030345.1:g.34161C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000243344.8:c.1387C>T MANE Select	ENSP00000243344.7:p.Pro463Ser
ENST00000652557.1:c.1387C>T	ENSP00000498617.1:p.Pro463Ser
ENST00000679356.1:c.1387C>T	ENSP00000506245.1:p.Pro463Ser
ENST00000679671.1:n.1500C>T
ENST00000679676.1:c.1276C>T	ENSP00000505492.1:p.Pro426Ser
ENST00000679799.1:c.1387C>T	ENSP00000505208.1:p.Pro463Ser
ENST00000679840.1:c.1387C>T	ENSP00000505248.1:p.Pro463Ser
ENST00000679931.1:c.*429C>T	ENSP00000505632.1:n.*429C>T
ENST00000679967.1:c.1387C>T	ENSP00000506607.1:p.Pro463Ser
ENST00000680225.1:n.646C>T
ENST00000680327.1:c.*429C>T	ENSP00000506639.1:n.*429C>T
ENST00000680448.1:c.1387C>T	ENSP00000505921.1:p.Pro463Ser
ENST00000680657.1:n.1498C>T
ENST00000680690.1:c.*639C>T	ENSP00000506121.1:n.*639C>T
ENST00000680888.1:c.1387C>T	ENSP00000506276.1:p.Pro463Ser
ENST00000680947.1:c.*659C>T	ENSP00000506496.1:n.*659C>T
ENST00000681024.1:c.1387C>T	ENSP00000506449.1:p.Pro463Ser
ENST00000681083.1:c.*1121C>T	ENSP00000506095.1:n.*1121C>T
ENST00000681167.1:n.1261C>T
ENST00000681483.1:c.1387C>T	ENSP00000505499.1:p.Pro463Ser
ENST00000681502.1:c.*811C>T	ENSP00000505644.1:n.*811C>T
ENST00000681606.1:c.1387C>T	ENSP00000505354.1:p.Pro463Ser
ENST00000681819.1:c.1387C>T	ENSP00000505673.1:p.Pro463Ser
ENST00000681952.1:c.1387C>T	ENSP00000506400.1:p.Pro463Ser
ENST00000243344.7:c.1387C>T	ENSP00000243344.7:p.Pro463Ser
NM_024753.4:c.1387C>T	NP_079029.3:p.Pro463Ser
XM_006712761.1:c.1387C>T	XP_006712824.1:p.Pro463Ser
XM_011511870.1:c.820C>T	XP_011510172.1:p.Pro274Ser
XM_011511871.1:c.637C>T	XP_011510173.1:p.Pro213Ser
XM_011511872.1:c.1387C>T	XP_011510174.1:p.Pro463Ser
XM_011511871.3:c.637C>T	XP_011510173.1:p.Pro213Ser
XM_011511872.2:c.1387C>T	XP_011510174.1:p.Pro463Ser
XM_017004967.1:c.1387C>T	XP_016860456.1:p.Pro463Ser
XM_017004968.2:c.733C>T	XP_016860457.1:p.Pro245Ser
XM_017004969.1:c.388C>T	XP_016860458.1:p.Pro130Ser
NM_024753.5:c.1387C>T MANE Select	NP_079029.3:p.Pro463Ser