Canonical Allele Identifier: CA1304775635

Gene: TTC21B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165857496G= , CM000664.2:g.165857496G=	GRCh38
NC_000002.11:g.166714006G= , CM000664.1:g.166714006G=	GRCh37
NC_000002.10:g.166422252G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000679356.1:c.*4267C=	ENSP00000506245.1:n.*4267C=
ENST00000679676.1:c.*4267C=	ENSP00000505492.1:n.*4267C=
ENST00000679931.1:c.*3602C=	ENSP00000505632.1:n.*3602C=
ENST00000679967.1:c.*4267C=	ENSP00000506607.1:n.*4267C=
ENST00000680249.1:n.3857C=
ENST00000680327.1:c.*7260C=	ENSP00000506639.1:n.*7260C=
ENST00000680657.1:n.6461C=
ENST00000680690.1:c.*7470C=	ENSP00000506121.1:n.*7470C=
ENST00000680888.1:c.*4267C=	ENSP00000506276.1:n.*4267C=
ENST00000680904.1:n.4722C=
ENST00000680947.1:c.*7490C=	ENSP00000506496.1:n.*7490C=
ENST00000681024.1:c.*8008C=	ENSP00000506449.1:n.*8008C=
ENST00000681083.1:c.*7949C=	ENSP00000506095.1:n.*7949C=
ENST00000681167.1:n.8096C=
ENST00000681483.1:c.*1370C=	ENSP00000505499.1:n.*1370C=
ENST00000681502.1:c.*11478C=	ENSP00000505644.1:n.*11478C=
ENST00000392695.6:c.1554C=
ENST00000486672.5:n.724C=
ENST00000489714.5:n.626C=
NR_045375.2:n.1576C=