Canonical Allele Identifier: CA1304775637
Gene: TTC21B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.165857499T= , CM000664.2:g.165857499T= GRCh38
NC_000002.11:g.166714009T= , CM000664.1:g.166714009T= GRCh37
NC_000002.10:g.166422255T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000679356.1:c.*4264A= ENSP00000506245.1:n.*4264A=
ENST00000679676.1:c.*4264A= ENSP00000505492.1:n.*4264A=
ENST00000679931.1:c.*3599A= ENSP00000505632.1:n.*3599A=
ENST00000679967.1:c.*4264A= ENSP00000506607.1:n.*4264A=
ENST00000680249.1:n.3854A=
ENST00000680327.1:c.*7257A= ENSP00000506639.1:n.*7257A=
ENST00000680657.1:n.6458A=
ENST00000680690.1:c.*7467A= ENSP00000506121.1:n.*7467A=
ENST00000680888.1:c.*4264A= ENSP00000506276.1:n.*4264A=
ENST00000680904.1:n.4719A=
ENST00000680947.1:c.*7487A= ENSP00000506496.1:n.*7487A=
ENST00000681024.1:c.*8005A= ENSP00000506449.1:n.*8005A=
ENST00000681083.1:c.*7946A= ENSP00000506095.1:n.*7946A=
ENST00000681167.1:n.8093A=
ENST00000681483.1:c.*1367A= ENSP00000505499.1:n.*1367A=
ENST00000681502.1:c.*11475A= ENSP00000505644.1:n.*11475A=
ENST00000392695.6:c.1551A=
ENST00000486672.5:n.721A=
ENST00000489714.5:n.623A=
NR_045375.2:n.1573A=