Canonical Allele Identifier: CA2068914708

Gene: TCTN2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123686865C= , CM000674.2:g.123686865C=	GRCh38
NC_000012.11:g.124171412C= , CM000674.1:g.124171412C=	GRCh37
NC_000012.10:g.122737365C=	NCBI36
NG_030442.1:g.20753C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303372.7:c.594C= MANE Select	ENSP00000304941.5:p.Phe198=
ENST00000679504.1:c.591C=	ENSP00000505006.1:p.Phe197=
ENST00000680500.1:c.594C=	ENSP00000506438.1:p.Phe198=
ENST00000680574.1:c.594C=	ENSP00000505356.1:p.Phe198=
ENST00000303372.6:c.594C=	ENSP00000304941.5:p.Phe198=
ENST00000426174.6:c.591C=	ENSP00000395171.2:p.Phe197=
NM_001143850.2:c.591C=	NP_001137322.1:p.Phe197=
NM_024809.4:c.594C=	NP_079085.2:p.Phe198=
XM_005253623.2:c.594C=	XP_005253680.1:p.Phe198=
XM_006719605.2:c.594C=	XP_006719668.1:p.Phe198=
XM_006719605.3:c.594C=	XP_006719668.1:p.Phe198=
XM_017019974.1:c.591C=	XP_016875463.1:p.Phe197=
XM_017019975.1:c.-192C=	XP_016875464.1:n.-192C=
NM_024809.5:c.594C= MANE Select	NP_079085.2:p.Phe198=
NM_001143850.3:c.591C=	NP_001137322.1:p.Phe197=