Canonical Allele Identifier: CA1941366

Gene: TTC21B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165876155A>T , CM000664.2:g.165876155A>T	GRCh38
NC_000002.11:g.166732665A>T , CM000664.1:g.166732665A>T	GRCh37
NC_000002.10:g.166440911A>T	NCBI36
NG_030345.1:g.82684T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_024753.5:c.3873+10T>A MANE Select	NP_079029.3:n.3873+10T>A
ENST00000243344.8:c.3873+10T>A MANE Select	ENSP00000243344.7:n.3873+10T>A
NM_024753.4:c.3873+10T>A	NP_079029.3:n.3873+10T>A
ENST00000243344.7:c.3873+10T>A	ENSP00000243344.7:n.3873+10T>A
ENST00000392695.6:c.773+10T>A
ENST00000652557.1:c.3805+4524T>A	ENSP00000498617.1:n.3805+4524T>A
ENST00000679356.1:c.3870+10T>A	ENSP00000506245.1:n.3870+10T>A
ENST00000679676.1:c.3762+10T>A	ENSP00000505492.1:n.3762+10T>A
ENST00000679799.1:c.3805+4524T>A	ENSP00000505208.1:n.3805+4524T>A
ENST00000679931.1:c.*2915+10T>A	ENSP00000505632.1:n.*2915+10T>A
ENST00000679967.1:c.3864+10T>A	ENSP00000506607.1:n.3864+10T>A
ENST00000680327.1:c.*2915+10T>A	ENSP00000506639.1:n.*2915+10T>A
ENST00000680657.1:n.3994T>A
ENST00000680690.1:c.*3125+10T>A	ENSP00000506121.1:n.*3125+10T>A
ENST00000680888.1:c.3873+10T>A	ENSP00000506276.1:n.3873+10T>A
ENST00000680947.1:c.*3145+10T>A	ENSP00000506496.1:n.*3145+10T>A
ENST00000681024.1:c.*3663+10T>A	ENSP00000506449.1:n.*3663+10T>A
ENST00000681083.1:c.*3604+10T>A	ENSP00000506095.1:n.*3604+10T>A
ENST00000681167.1:n.3751+10T>A
ENST00000681483.1:c.*683+10T>A	ENSP00000505499.1:n.*683+10T>A
ENST00000681502.1:c.*7133+10T>A	ENSP00000505644.1:n.*7133+10T>A
ENST00000681819.1:c.*683+10T>A	ENSP00000505673.1:n.*683+10T>A
ENST00000681952.1:c.3873+10T>A	ENSP00000506400.1:n.3873+10T>A
XM_011511870.1:c.3306+10T>A	XP_011510172.1:n.3306+10T>A
XM_011511871.1:c.3123+10T>A	XP_011510173.1:n.3123+10T>A
XM_011511871.3:c.3123+10T>A	XP_011510173.1:n.3123+10T>A
XM_011511872.2:c.*1075+10T>A	XP_011510174.1:n.*1075+10T>A
XM_017004968.2:c.3219+10T>A	XP_016860457.1:n.3219+10T>A
XM_017004969.1:c.2874+10T>A	XP_016860458.1:n.2874+10T>A