Canonical Allele Identifier: CA387161581

Gene: TCTN2

Linked Data

• MyVariant Identifiers: chr12:g.124171440G>A (hg19) ; chr12:g.123686893G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123686893G>A , CM000674.2:g.123686893G>A	GRCh38
NC_000012.11:g.124171440G>A , CM000674.1:g.124171440G>A	GRCh37
NC_000012.10:g.122737393G>A	NCBI36
NG_030442.1:g.20781G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303372.7:c.622G>A MANE Select	ENSP00000304941.5:p.Gly208Arg
ENST00000679504.1:c.619G>A	ENSP00000505006.1:p.Gly207Arg
ENST00000680500.1:c.622G>A	ENSP00000506438.1:p.Gly208Arg
ENST00000680574.1:c.622G>A	ENSP00000505356.1:p.Gly208Arg
ENST00000303372.6:c.622G>A	ENSP00000304941.5:p.Gly208Arg
ENST00000426174.6:c.619G>A	ENSP00000395171.2:p.Gly207Arg
NM_001143850.2:c.619G>A	NP_001137322.1:p.Gly207Arg
NM_024809.4:c.622G>A	NP_079085.2:p.Gly208Arg
XM_005253623.2:c.622G>A	XP_005253680.1:p.Gly208Arg
XM_006719605.2:c.622G>A	XP_006719668.1:p.Gly208Arg
XM_006719605.3:c.622G>A	XP_006719668.1:p.Gly208Arg
XM_017019974.1:c.619G>A	XP_016875463.1:p.Gly207Arg
XM_017019975.1:c.-164G>A	XP_016875464.1:n.-164G>A
NM_024809.5:c.622G>A MANE Select	NP_079085.2:p.Gly208Arg
NM_001143850.3:c.619G>A	NP_001137322.1:p.Gly207Arg