Canonical Allele Identifier: CA6861181

Gene: TCTN2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123696438C>T , CM000674.2:g.123696438C>T	GRCh38
NC_000012.11:g.124180985C>T , CM000674.1:g.124180985C>T	GRCh37
NC_000012.10:g.122746938C>T	NCBI36
NG_030442.1:g.30326C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_024809.5:c.1336C>T MANE Select	NP_079085.2:p.Arg446Ter
ENST00000303372.7:c.1336C>T MANE Select	ENSP00000304941.5:p.Arg446Ter
NM_001143850.2:c.1333C>T	NP_001137322.1:p.Arg445Ter
NM_001143850.3:c.1333C>T	NP_001137322.1:p.Arg445Ter
NM_024809.4:c.1336C>T	NP_079085.2:p.Arg446Ter
ENST00000303372.6:c.1336C>T	ENSP00000304941.5:p.Arg446Ter
ENST00000426174.6:c.1333C>T	ENSP00000395171.2:p.Arg445Ter
ENST00000543998.1:n.1399C>T
ENST00000679504.1:c.1333C>T	ENSP00000505006.1:p.Arg445Ter
ENST00000680394.1:n.437C>T
ENST00000680500.1:c.1336C>T	ENSP00000506438.1:p.Arg446Ter
ENST00000680574.1:c.1201C>T	ENSP00000505356.1:p.Arg401Ter
XM_005253623.2:c.1201C>T	XP_005253680.1:p.Arg401Ter
XM_006719605.2:c.1336C>T	XP_006719668.1:p.Arg446Ter
XM_006719605.3:c.1336C>T	XP_006719668.1:p.Arg446Ter
XM_011538748.1:c.424C>T	XP_011537050.1:p.Arg142Ter
XM_017019974.1:c.1198C>T	XP_016875463.1:p.Arg400Ter
XM_017019975.1:c.424C>T	XP_016875464.1:p.Arg142Ter