Canonical Allele Identifier: CA387161385

Gene: TCTN2

Linked Data

• MyVariant Identifiers: chr12:g.124171410T>A (hg19) ; chr12:g.123686863T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123686863T>A , CM000674.2:g.123686863T>A	GRCh38
NC_000012.11:g.124171410T>A , CM000674.1:g.124171410T>A	GRCh37
NC_000012.10:g.122737363T>A	NCBI36
NG_030442.1:g.20751T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303372.7:c.592T>A MANE Select	ENSP00000304941.5:p.Phe198Ile
ENST00000679504.1:c.589T>A	ENSP00000505006.1:p.Phe197Ile
ENST00000680500.1:c.592T>A	ENSP00000506438.1:p.Phe198Ile
ENST00000680574.1:c.592T>A	ENSP00000505356.1:p.Phe198Ile
ENST00000303372.6:c.592T>A	ENSP00000304941.5:p.Phe198Ile
ENST00000426174.6:c.589T>A	ENSP00000395171.2:p.Phe197Ile
NM_001143850.2:c.589T>A	NP_001137322.1:p.Phe197Ile
NM_024809.4:c.592T>A	NP_079085.2:p.Phe198Ile
XM_005253623.2:c.592T>A	XP_005253680.1:p.Phe198Ile
XM_006719605.2:c.592T>A	XP_006719668.1:p.Phe198Ile
XM_006719605.3:c.592T>A	XP_006719668.1:p.Phe198Ile
XM_017019974.1:c.589T>A	XP_016875463.1:p.Phe197Ile
XM_017019975.1:c.-194T>A	XP_016875464.1:n.-194T>A
NM_024809.5:c.592T>A MANE Select	NP_079085.2:p.Phe198Ile
NM_001143850.3:c.589T>A	NP_001137322.1:p.Phe197Ile