Canonical Allele Identifier: CA387156659

Gene: TCTN2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123673613A>G , CM000674.2:g.123673613A>G	GRCh38
NC_000012.11:g.124158160A>G , CM000674.1:g.124158160A>G	GRCh37
NC_000012.10:g.122724113A>G	NCBI36
NG_030442.1:g.7501A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_024809.5:c.268-2A>G MANE Select	NP_079085.2:n.268-2A>G
ENST00000303372.7:c.268-2A>G MANE Select	ENSP00000304941.5:n.268-2A>G
NM_001143850.2:c.268-5A>G	NP_001137322.1:n.268-5A>G
NM_001143850.3:c.268-5A>G	NP_001137322.1:n.268-5A>G
NM_024809.4:c.268-2A>G	NP_079085.2:n.268-2A>G
ENST00000303372.6:c.268-2A>G	ENSP00000304941.5:n.268-2A>G
ENST00000426174.6:c.268-5A>G	ENSP00000395171.2:n.268-5A>G
ENST00000541523.1:c.*111-2A>G	ENSP00000437644.1:n.*111-2A>G
ENST00000679504.1:c.268-5A>G	ENSP00000505006.1:n.268-5A>G
ENST00000680500.1:c.268-2A>G	ENSP00000506438.1:n.268-2A>G
ENST00000680574.1:c.268-2A>G	ENSP00000505356.1:n.268-2A>G
XM_005253623.2:c.268-2A>G	XP_005253680.1:n.268-2A>G
XM_006719605.2:c.268-2A>G	XP_006719668.1:n.268-2A>G
XM_006719605.3:c.268-2A>G	XP_006719668.1:n.268-2A>G
XM_017019974.1:c.268-5A>G	XP_016875463.1:n.268-5A>G
XM_017019975.1:c.-515-5A>G	XP_016875464.1:n.-515-5A>G