Canonical Allele Identifier: CA2068914368

Gene: TCTN2

Linked Data

• dbSNP Id: rs1955970937

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123686680del , CM000674.2:g.123686680del	GRCh38
NC_000012.11:g.124171227del , CM000674.1:g.124171227del	GRCh37
NC_000012.10:g.122737180del	NCBI36
NG_030442.1:g.20568del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303372.7:c.565-156del MANE Select	ENSP00000304941.5:n.565-156del
ENST00000679504.1:c.562-156del	ENSP00000505006.1:n.562-156del
ENST00000680500.1:c.565-156del	ENSP00000506438.1:n.565-156del
ENST00000680574.1:c.565-156del	ENSP00000505356.1:n.565-156del
ENST00000303372.6:c.565-156del	ENSP00000304941.5:n.565-156del
ENST00000426174.6:c.562-156del	ENSP00000395171.2:n.562-156del
NM_001143850.2:c.562-156del	NP_001137322.1:n.562-156del
NM_024809.4:c.565-156del	NP_079085.2:n.565-156del
XM_005253623.2:c.565-156del	XP_005253680.1:n.565-156del
XM_006719605.2:c.565-156del	XP_006719668.1:n.565-156del
XM_006719605.3:c.565-156del	XP_006719668.1:n.565-156del
XM_017019974.1:c.562-156del	XP_016875463.1:n.562-156del
XM_017019975.1:c.-221-156del	XP_016875464.1:n.-221-156del
NM_024809.5:c.565-156del MANE Select	NP_079085.2:n.565-156del
NM_001143850.3:c.562-156del	NP_001137322.1:n.562-156del