Canonical Allele Identifier: CA279354

Gene: TCTN2

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123671316dup , CM000674.2:g.123671316dup	GRCh38
NC_000012.11:g.124155863dup , CM000674.1:g.124155863dup	GRCh37
NC_000012.10:g.122721816dup	NCBI36
NG_030442.1:g.5204dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303372.7:c.76dup MANE Select	ENSP00000304941.5:p.Asp26GlyfsTer?
ENST00000679504.1:c.76dup	ENSP00000505006.1:p.Asp26GlyfsTer?
ENST00000680500.1:c.76dup	ENSP00000506438.1:p.Asp26GlyfsTer?
ENST00000680574.1:c.76dup	ENSP00000505356.1:p.Asp26GlyfsTer?
ENST00000303372.6:c.76dup	ENSP00000304941.5:p.Asp26GlyfsTer?
ENST00000426174.6:c.76dup	ENSP00000395171.2:p.Asp26GlyfsTer?
ENST00000541523.1:c.76dup	ENSP00000437644.1:p.Asp26GlyfsTer?
NM_001143850.2:c.76dup	NP_001137322.1:p.Asp26GlyfsTer?
NM_024809.4:c.76dup	NP_079085.2:p.Asp26GlyfsTer?
XM_005253623.2:c.76dup	XP_005253680.1:p.Asp26GlyfsTer?
XM_006719605.2:c.76dup	XP_006719668.1:p.Asp26GlyfsTer?
XM_006719605.3:c.76dup	XP_006719668.1:p.Asp26GlyfsTer?
XM_017019974.1:c.76dup	XP_016875463.1:p.Asp26GlyfsTer?
XM_017019975.1:c.-707dup	XP_016875464.1:n.-707dup
NM_024809.5:c.76dup MANE Select	NP_079085.2:p.Asp26GlyfsTer?
NM_001143850.3:c.76dup	NP_001137322.1:p.Asp26GlyfsTer?