Canonical Allele Identifier: CA2068914078

Gene: TCTN2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123686487_123686491delinsCAATT , CM000674.2:g.123686487_123686491delinsCAATT	GRCh38
NC_000012.11:g.124171034_124171038delinsCAATT , CM000674.1:g.124171034_124171038delinsCAATT	GRCh37
NC_000012.10:g.122736987_122736991delinsCAATT	NCBI36
NG_030442.1:g.20375_20379delinsCAATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303372.7:c.565-349_565-345delinsCAATT MANE Select	ENSP00000304941.5:n.565-349_565-345delinsCAATT
ENST00000679504.1:c.562-349_562-345delinsCAATT	ENSP00000505006.1:n.562-349_562-345delinsCAATT
ENST00000680500.1:c.565-349_565-345delinsCAATT	ENSP00000506438.1:n.565-349_565-345delinsCAATT
ENST00000680574.1:c.565-349_565-345delinsCAATT	ENSP00000505356.1:n.565-349_565-345delinsCAATT
ENST00000303372.6:c.565-349_565-345delinsCAATT	ENSP00000304941.5:n.565-349_565-345delinsCAATT
ENST00000426174.6:c.562-349_562-345delinsCAATT	ENSP00000395171.2:n.562-349_562-345delinsCAATT
NM_001143850.2:c.562-349_562-345delinsCAATT	NP_001137322.1:n.562-349_562-345delinsCAATT
NM_024809.4:c.565-349_565-345delinsCAATT	NP_079085.2:n.565-349_565-345delinsCAATT
XM_005253623.2:c.565-349_565-345delinsCAATT	XP_005253680.1:n.565-349_565-345delinsCAATT
XM_006719605.2:c.565-349_565-345delinsCAATT	XP_006719668.1:n.565-349_565-345delinsCAATT
XM_006719605.3:c.565-349_565-345delinsCAATT	XP_006719668.1:n.565-349_565-345delinsCAATT
XM_017019974.1:c.562-349_562-345delinsCAATT	XP_016875463.1:n.562-349_562-345delinsCAATT
XM_017019975.1:c.-221-349_-221-345delinsCAATT	XP_016875464.1:n.-221-349_-221-345delinsCAATT
NM_024809.5:c.565-349_565-345delinsCAATT MANE Select	NP_079085.2:n.565-349_565-345delinsCAATT
NM_001143850.3:c.562-349_562-345delinsCAATT	NP_001137322.1:n.562-349_562-345delinsCAATT