Canonical Allele Identifier: CA1304775646

Gene: TTC21B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165857525_165857526delinsCT , CM000664.2:g.165857525_165857526delinsCT	GRCh38
NC_000002.11:g.166714035_166714036delinsCT , CM000664.1:g.166714035_166714036delinsCT	GRCh37
NC_000002.10:g.166422281_166422282delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000679356.1:c.*4237_*4238delinsAG	ENSP00000506245.1:n.*4237_*4238delinsAG
ENST00000679676.1:c.*4237_*4238delinsAG	ENSP00000505492.1:n.*4237_*4238delinsAG
ENST00000679931.1:c.*3572_*3573delinsAG	ENSP00000505632.1:n.*3572_*3573delinsAG
ENST00000679967.1:c.*4237_*4238delinsAG	ENSP00000506607.1:n.*4237_*4238delinsAG
ENST00000680249.1:n.3827_3828delinsAG
ENST00000680327.1:c.*7230_*7231delinsAG	ENSP00000506639.1:n.*7230_*7231delinsAG
ENST00000680657.1:n.6431_6432delinsAG
ENST00000680690.1:c.*7440_*7441delinsAG	ENSP00000506121.1:n.*7440_*7441delinsAG
ENST00000680888.1:c.*4237_*4238delinsAG	ENSP00000506276.1:n.*4237_*4238delinsAG
ENST00000680904.1:n.4692_4693delinsAG
ENST00000680947.1:c.*7460_*7461delinsAG	ENSP00000506496.1:n.*7460_*7461delinsAG
ENST00000681024.1:c.*7978_*7979delinsAG	ENSP00000506449.1:n.*7978_*7979delinsAG
ENST00000681083.1:c.*7919_*7920delinsAG	ENSP00000506095.1:n.*7919_*7920delinsAG
ENST00000681167.1:n.8066_8067delinsAG
ENST00000681483.1:c.*1340_*1341delinsAG	ENSP00000505499.1:n.*1340_*1341delinsAG
ENST00000681502.1:c.*11448_*11449delinsAG	ENSP00000505644.1:n.*11448_*11449delinsAG...
ENST00000681952.1:c.*579_*580delinsAG	ENSP00000506400.1:n.*579_*580delinsAG
ENST00000392695.6:c.1524_1525delinsAG
ENST00000486672.5:n.694_695delinsAG
ENST00000489714.5:n.596_597delinsAG
NR_045375.2:n.1546_1547delinsAG