Canonical Allele Identifier: CA2068986552

Gene: TCTN2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123706829C= , CM000674.2:g.123706829C=	GRCh38
NC_000012.11:g.124191376C= , CM000674.1:g.124191376C=	GRCh37
NC_000012.10:g.122757329C=	NCBI36
NG_030442.1:g.40717C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303372.7:c.1873C= MANE Select	ENSP00000304941.5:p.Gln625=
ENST00000679504.1:c.1870C=	ENSP00000505006.1:p.Gln624=
ENST00000680394.1:n.974C=
ENST00000680500.1:c.*245C=	ENSP00000506438.1:n.*245C=
ENST00000680574.1:c.1738C=	ENSP00000505356.1:p.Gln580=
ENST00000303372.6:c.1873C=	ENSP00000304941.5:p.Gln625=
ENST00000426174.6:c.1870C=	ENSP00000395171.2:p.Gln624=
ENST00000543998.1:n.2645C=
NM_001143850.2:c.1870C=	NP_001137322.1:p.Gln624=
NM_024809.4:c.1873C=	NP_079085.2:p.Gln625=
XM_005253623.2:c.1738C=	XP_005253680.1:p.Gln580=
XM_006719605.2:c.1873C=	XP_006719668.1:p.Gln625=
XM_011538748.1:c.961C=	XP_011537050.1:p.Gln321=
XM_006719605.3:c.1873C=	XP_006719668.1:p.Gln625=
XM_017019974.1:c.1735C=	XP_016875463.1:p.Gln579=
XM_017019975.1:c.961C=	XP_016875464.1:p.Gln321=
NM_024809.5:c.1873C= MANE Select	NP_079085.2:p.Gln625=
NM_001143850.3:c.1870C=	NP_001137322.1:p.Gln624=