Canonical Allele Identifier: CA387161568

Gene: TCTN2

Linked Data

• MyVariant Identifiers: chr12:g.124171438T>G (hg19) ; chr12:g.123686891T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123686891T>G , CM000674.2:g.123686891T>G	GRCh38
NC_000012.11:g.124171438T>G , CM000674.1:g.124171438T>G	GRCh37
NC_000012.10:g.122737391T>G	NCBI36
NG_030442.1:g.20779T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303372.7:c.620T>G MANE Select	ENSP00000304941.5:p.Phe207Cys
ENST00000679504.1:c.617T>G	ENSP00000505006.1:p.Phe206Cys
ENST00000680500.1:c.620T>G	ENSP00000506438.1:p.Phe207Cys
ENST00000680574.1:c.620T>G	ENSP00000505356.1:p.Phe207Cys
ENST00000303372.6:c.620T>G	ENSP00000304941.5:p.Phe207Cys
ENST00000426174.6:c.617T>G	ENSP00000395171.2:p.Phe206Cys
NM_001143850.2:c.617T>G	NP_001137322.1:p.Phe206Cys
NM_024809.4:c.620T>G	NP_079085.2:p.Phe207Cys
XM_005253623.2:c.620T>G	XP_005253680.1:p.Phe207Cys
XM_006719605.2:c.620T>G	XP_006719668.1:p.Phe207Cys
XM_006719605.3:c.620T>G	XP_006719668.1:p.Phe207Cys
XM_017019974.1:c.617T>G	XP_016875463.1:p.Phe206Cys
XM_017019975.1:c.-166T>G	XP_016875464.1:n.-166T>G
NM_024809.5:c.620T>G MANE Select	NP_079085.2:p.Phe207Cys
NM_001143850.3:c.617T>G	NP_001137322.1:p.Phe206Cys