Canonical Allele Identifier: CA2068914187

Gene: TCTN2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123686550T= , CM000674.2:g.123686550T=	GRCh38
NC_000012.11:g.124171097T= , CM000674.1:g.124171097T=	GRCh37
NC_000012.10:g.122737050T=	NCBI36
NG_030442.1:g.20438T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303372.7:c.565-286T= MANE Select	ENSP00000304941.5:n.565-286T=
ENST00000679504.1:c.562-286T=	ENSP00000505006.1:n.562-286T=
ENST00000680500.1:c.565-286T=	ENSP00000506438.1:n.565-286T=
ENST00000680574.1:c.565-286T=	ENSP00000505356.1:n.565-286T=
ENST00000303372.6:c.565-286T=	ENSP00000304941.5:n.565-286T=
ENST00000426174.6:c.562-286T=	ENSP00000395171.2:n.562-286T=
NM_001143850.2:c.562-286T=	NP_001137322.1:n.562-286T=
NM_024809.4:c.565-286T=	NP_079085.2:n.565-286T=
XM_005253623.2:c.565-286T=	XP_005253680.1:n.565-286T=
XM_006719605.2:c.565-286T=	XP_006719668.1:n.565-286T=
XM_006719605.3:c.565-286T=	XP_006719668.1:n.565-286T=
XM_017019974.1:c.562-286T=	XP_016875463.1:n.562-286T=
XM_017019975.1:c.-221-286T=	XP_016875464.1:n.-221-286T=
NM_024809.5:c.565-286T= MANE Select	NP_079085.2:n.565-286T=
NM_001143850.3:c.562-286T=	NP_001137322.1:n.562-286T=