Canonical Allele Identifier: CA2068914718

Gene: TCTN2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123686870G= , CM000674.2:g.123686870G=	GRCh38
NC_000012.11:g.124171417G= , CM000674.1:g.124171417G=	GRCh37
NC_000012.10:g.122737370G=	NCBI36
NG_030442.1:g.20758G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303372.7:c.599G= MANE Select	ENSP00000304941.5:p.Arg200=
ENST00000679504.1:c.596G=	ENSP00000505006.1:p.Arg199=
ENST00000680500.1:c.599G=	ENSP00000506438.1:p.Arg200=
ENST00000680574.1:c.599G=	ENSP00000505356.1:p.Arg200=
ENST00000303372.6:c.599G=	ENSP00000304941.5:p.Arg200=
ENST00000426174.6:c.596G=	ENSP00000395171.2:p.Arg199=
NM_001143850.2:c.596G=	NP_001137322.1:p.Arg199=
NM_024809.4:c.599G=	NP_079085.2:p.Arg200=
XM_005253623.2:c.599G=	XP_005253680.1:p.Arg200=
XM_006719605.2:c.599G=	XP_006719668.1:p.Arg200=
XM_006719605.3:c.599G=	XP_006719668.1:p.Arg200=
XM_017019974.1:c.596G=	XP_016875463.1:p.Arg199=
XM_017019975.1:c.-187G=	XP_016875464.1:n.-187G=
NM_024809.5:c.599G= MANE Select	NP_079085.2:p.Arg200=
NM_001143850.3:c.596G=	NP_001137322.1:p.Arg199=