Canonical Allele Identifier: CA2068983465

Gene: TCTN2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123704545T= , CM000674.2:g.123704545T=	GRCh38
NC_000012.11:g.124189092T= , CM000674.1:g.124189092T=	GRCh37
NC_000012.10:g.122755045T=	NCBI36
NG_030442.1:g.38433T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303372.7:c.1626T= MANE Select	ENSP00000304941.5:p.Pro542=
ENST00000679504.1:c.1623T=	ENSP00000505006.1:p.Pro541=
ENST00000680394.1:n.727T=
ENST00000680500.1:c.1744T=	ENSP00000506438.1:p.Ter582=
ENST00000680574.1:c.1491T=	ENSP00000505356.1:p.Pro497=
ENST00000303372.6:c.1626T=	ENSP00000304941.5:p.Pro542=
ENST00000426174.6:c.1623T=	ENSP00000395171.2:p.Pro541=
ENST00000543998.1:n.2398T=
NM_001143850.2:c.1623T=	NP_001137322.1:p.Pro541=
NM_024809.4:c.1626T=	NP_079085.2:p.Pro542=
XM_005253623.2:c.1491T=	XP_005253680.1:p.Pro497=
XM_006719605.2:c.1626T=	XP_006719668.1:p.Pro542=
XM_011538748.1:c.714T=	XP_011537050.1:p.Pro238=
XM_006719605.3:c.1626T=	XP_006719668.1:p.Pro542=
XM_017019974.1:c.1488T=	XP_016875463.1:p.Pro496=
XM_017019975.1:c.714T=	XP_016875464.1:p.Pro238=
NM_024809.5:c.1626T= MANE Select	NP_079085.2:p.Pro542=
NM_001143850.3:c.1623T=	NP_001137322.1:p.Pro541=