Canonical Allele Identifier: CA2621689116

Gene: TCTN2

Linked Data

• gnomAD v4: 12-123686783-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123686785del , CM000674.2:g.123686785del	GRCh38
NC_000012.11:g.124171332del , CM000674.1:g.124171332del	GRCh37
NC_000012.10:g.122737285del	NCBI36
NG_030442.1:g.20673del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303372.7:c.565-51del MANE Select	ENSP00000304941.5:n.565-51del
ENST00000679504.1:c.562-51del	ENSP00000505006.1:n.562-51del
ENST00000680500.1:c.565-51del	ENSP00000506438.1:n.565-51del
ENST00000680574.1:c.565-51del	ENSP00000505356.1:n.565-51del
ENST00000303372.6:c.565-51del	ENSP00000304941.5:n.565-51del
ENST00000426174.6:c.562-51del	ENSP00000395171.2:n.562-51del
NM_001143850.2:c.562-51del	NP_001137322.1:n.562-51del
NM_024809.4:c.565-51del	NP_079085.2:n.565-51del
XM_005253623.2:c.565-51del	XP_005253680.1:n.565-51del
XM_006719605.2:c.565-51del	XP_006719668.1:n.565-51del
XM_006719605.3:c.565-51del	XP_006719668.1:n.565-51del
XM_017019974.1:c.562-51del	XP_016875463.1:n.562-51del
XM_017019975.1:c.-221-51del	XP_016875464.1:n.-221-51del
NM_024809.5:c.565-51del MANE Select	NP_079085.2:n.565-51del
NM_001143850.3:c.562-51del	NP_001137322.1:n.562-51del