Canonical Allele Identifier: CA6861261

Gene: TCTN2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123699777G>A , CM000674.2:g.123699777G>A	GRCh38
NC_000012.11:g.124184324G>A , CM000674.1:g.124184324G>A	GRCh37
NC_000012.10:g.122750277G>A	NCBI36
NG_030442.1:g.33665G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_024809.5:c.1579G>A MANE Select	NP_079085.2:p.Ala527Thr
ENST00000303372.7:c.1579G>A MANE Select	ENSP00000304941.5:p.Ala527Thr
NM_001143850.2:c.1576G>A	NP_001137322.1:p.Ala526Thr
NM_001143850.3:c.1576G>A	NP_001137322.1:p.Ala526Thr
NM_024809.4:c.1579G>A	NP_079085.2:p.Ala527Thr
ENST00000303372.6:c.1579G>A	ENSP00000304941.5:p.Ala527Thr
ENST00000426174.6:c.1576G>A	ENSP00000395171.2:p.Ala526Thr
ENST00000543998.1:n.2233G>A
ENST00000679504.1:c.1576G>A	ENSP00000505006.1:p.Ala526Thr
ENST00000680394.1:n.680G>A
ENST00000680500.1:c.1579G>A	ENSP00000506438.1:p.Ala527Thr
ENST00000680574.1:c.1444G>A	ENSP00000505356.1:p.Ala482Thr
XM_005253623.2:c.1444G>A	XP_005253680.1:p.Ala482Thr
XM_006719605.2:c.1579G>A	XP_006719668.1:p.Ala527Thr
XM_006719605.3:c.1579G>A	XP_006719668.1:p.Ala527Thr
XM_011538748.1:c.667G>A	XP_011537050.1:p.Ala223Thr
XM_017019974.1:c.1441G>A	XP_016875463.1:p.Ala481Thr
XM_017019975.1:c.667G>A	XP_016875464.1:p.Ala223Thr