Canonical Allele Identifier: CA387155074

Gene: TCTN2

Linked Data

• MyVariant Identifiers: chr12:g.124156111G>T (hg19) ; chr12:g.123671564G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123671564G>T , CM000674.2:g.123671564G>T	GRCh38
NC_000012.11:g.124156111G>T , CM000674.1:g.124156111G>T	GRCh37
NC_000012.10:g.122722064G>T	NCBI36
NG_030442.1:g.5452G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303372.7:c.140G>T MANE Select	ENSP00000304941.5:p.Gly47Val
ENST00000679504.1:c.140G>T	ENSP00000505006.1:p.Gly47Val
ENST00000680500.1:c.140G>T	ENSP00000506438.1:p.Gly47Val
ENST00000680574.1:c.140G>T	ENSP00000505356.1:p.Gly47Val
ENST00000303372.6:c.140G>T	ENSP00000304941.5:p.Gly47Val
ENST00000426174.6:c.140G>T	ENSP00000395171.2:p.Gly47Val
ENST00000541523.1:c.166G>T	ENSP00000437644.1:p.Glu56Ter
NM_001143850.2:c.140G>T	NP_001137322.1:p.Gly47Val
NM_024809.4:c.140G>T	NP_079085.2:p.Gly47Val
XM_005253623.2:c.140G>T	XP_005253680.1:p.Gly47Val
XM_006719605.2:c.140G>T	XP_006719668.1:p.Gly47Val
XM_006719605.3:c.140G>T	XP_006719668.1:p.Gly47Val
XM_017019974.1:c.140G>T	XP_016875463.1:p.Gly47Val
XM_017019975.1:c.-643G>T	XP_016875464.1:n.-643G>T
NM_024809.5:c.140G>T MANE Select	NP_079085.2:p.Gly47Val
NM_001143850.3:c.140G>T	NP_001137322.1:p.Gly47Val