Canonical Allele Identifier: CA1941397

Gene: TTC21B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165880666T>C , CM000664.2:g.165880666T>C	GRCh38
NC_000002.11:g.166737176T>C , CM000664.1:g.166737176T>C	GRCh37
NC_000002.10:g.166445422T>C	NCBI36
NG_030345.1:g.78173A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_024753.5:c.3805+13A>G MANE Select	NP_079029.3:n.3805+13A>G
ENST00000243344.8:c.3805+13A>G MANE Select	ENSP00000243344.7:n.3805+13A>G
NM_024753.4:c.3805+13A>G	NP_079029.3:n.3805+13A>G
ENST00000243344.7:c.3805+13A>G	ENSP00000243344.7:n.3805+13A>G
ENST00000392695.6:c.705+13A>G
ENST00000497425.1:n.283+13A>G
ENST00000497425.2:n.927A>G
ENST00000652557.1:c.3805+13A>G	ENSP00000498617.1:n.3805+13A>G
ENST00000679356.1:c.3802+13A>G	ENSP00000506245.1:n.3802+13A>G
ENST00000679676.1:c.3694+13A>G	ENSP00000505492.1:n.3694+13A>G
ENST00000679799.1:c.3805+13A>G	ENSP00000505208.1:n.3805+13A>G
ENST00000679840.1:c.3818A>G	ENSP00000505248.1:p.Asn1273Ser
ENST00000679931.1:c.*2847+13A>G	ENSP00000505632.1:n.*2847+13A>G
ENST00000679967.1:c.3796+13A>G	ENSP00000506607.1:n.3796+13A>G
ENST00000680327.1:c.*2847+13A>G	ENSP00000506639.1:n.*2847+13A>G
ENST00000680657.1:n.3916+13A>G
ENST00000680690.1:c.*3057+13A>G	ENSP00000506121.1:n.*3057+13A>G
ENST00000680888.1:c.3805+13A>G	ENSP00000506276.1:n.3805+13A>G
ENST00000680925.1:n.1848A>G
ENST00000680947.1:c.*3077+13A>G	ENSP00000506496.1:n.*3077+13A>G
ENST00000681024.1:c.3805+13A>G	ENSP00000506449.1:n.3805+13A>G
ENST00000681083.1:c.*3536+13A>G	ENSP00000506095.1:n.*3536+13A>G
ENST00000681167.1:n.3683+13A>G
ENST00000681483.1:c.*615+13A>G	ENSP00000505499.1:n.*615+13A>G
ENST00000681502.1:c.*7065+13A>G	ENSP00000505644.1:n.*7065+13A>G
ENST00000681819.1:c.*615+13A>G	ENSP00000505673.1:n.*615+13A>G
ENST00000681952.1:c.3805+13A>G	ENSP00000506400.1:n.3805+13A>G
XM_011511870.1:c.3238+13A>G	XP_011510172.1:n.3238+13A>G
XM_011511871.1:c.3055+13A>G	XP_011510173.1:n.3055+13A>G
XM_011511871.3:c.3055+13A>G	XP_011510173.1:n.3055+13A>G
XM_011511872.2:c.*1007+13A>G	XP_011510174.1:n.*1007+13A>G
XM_017004967.1:c.3805+13A>G	XP_016860456.1:n.3805+13A>G
XM_017004968.2:c.3151+13A>G	XP_016860457.1:n.3151+13A>G
XM_017004969.1:c.2806+13A>G	XP_016860458.1:n.2806+13A>G