Canonical Allele Identifier: CA2068962123

Gene: TCTN2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123671402C= , CM000674.2:g.123671402C=	GRCh38
NC_000012.11:g.124155949C= , CM000674.1:g.124155949C=	GRCh37
NC_000012.10:g.122721902C=	NCBI36
NG_030442.1:g.5290C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303372.7:c.82+80C= MANE Select	ENSP00000304941.5:n.82+80C=
ENST00000679504.1:c.82+80C=	ENSP00000505006.1:n.82+80C=
ENST00000680500.1:c.82+80C=	ENSP00000506438.1:n.82+80C=
ENST00000680574.1:c.82+80C=	ENSP00000505356.1:n.82+80C=
ENST00000303372.6:c.82+80C=	ENSP00000304941.5:n.82+80C=
ENST00000426174.6:c.82+80C=	ENSP00000395171.2:n.82+80C=
ENST00000541523.1:c.108+54C=	ENSP00000437644.1:n.108+54C=
NM_001143850.2:c.82+80C=	NP_001137322.1:n.82+80C=
NM_024809.4:c.82+80C=	NP_079085.2:n.82+80C=
XM_005253623.2:c.82+80C=	XP_005253680.1:n.82+80C=
XM_006719605.2:c.82+80C=	XP_006719668.1:n.82+80C=
XM_006719605.3:c.82+80C=	XP_006719668.1:n.82+80C=
XM_017019974.1:c.82+80C=	XP_016875463.1:n.82+80C=
XM_017019975.1:c.-701+80C=	XP_016875464.1:n.-701+80C=
NM_024809.5:c.82+80C= MANE Select	NP_079085.2:n.82+80C=
NM_001143850.3:c.82+80C=	NP_001137322.1:n.82+80C=