Canonical Allele Identifier: CA2068986561

Gene: TCTN2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123706833T= , CM000674.2:g.123706833T=	GRCh38
NC_000012.11:g.124191380T= , CM000674.1:g.124191380T=	GRCh37
NC_000012.10:g.122757333T=	NCBI36
NG_030442.1:g.40721T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303372.7:c.1877T= MANE Select	ENSP00000304941.5:p.Leu626=
ENST00000679504.1:c.1874T=	ENSP00000505006.1:p.Leu625=
ENST00000680394.1:n.978T=
ENST00000680500.1:c.*249T=	ENSP00000506438.1:n.*249T=
ENST00000680574.1:c.1742T=	ENSP00000505356.1:p.Leu581=
ENST00000303372.6:c.1877T=	ENSP00000304941.5:p.Leu626=
ENST00000426174.6:c.1874T=	ENSP00000395171.2:p.Leu625=
ENST00000543998.1:n.2649T=
NM_001143850.2:c.1874T=	NP_001137322.1:p.Leu625=
NM_024809.4:c.1877T=	NP_079085.2:p.Leu626=
XM_005253623.2:c.1742T=	XP_005253680.1:p.Leu581=
XM_006719605.2:c.1877T=	XP_006719668.1:p.Leu626=
XM_011538748.1:c.965T=	XP_011537050.1:p.Leu322=
XM_006719605.3:c.1877T=	XP_006719668.1:p.Leu626=
XM_017019974.1:c.1739T=	XP_016875463.1:p.Leu580=
XM_017019975.1:c.965T=	XP_016875464.1:p.Leu322=
NM_024809.5:c.1877T= MANE Select	NP_079085.2:p.Leu626=
NM_001143850.3:c.1874T=	NP_001137322.1:p.Leu625=