Canonical Allele Identifier: CA2068962156
Gene: TCTN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.123671477C= , CM000674.2:g.123671477C= GRCh38
NC_000012.11:g.124156024C= , CM000674.1:g.124156024C= GRCh37
NC_000012.10:g.122721977C= NCBI36
NG_030442.1:g.5365C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000303372.7:c.83-30C= MANE Select ENSP00000304941.5:n.83-30C=
ENST00000679504.1:c.83-30C= ENSP00000505006.1:n.83-30C=
ENST00000680500.1:c.83-30C= ENSP00000506438.1:n.83-30C=
ENST00000680574.1:c.83-30C= ENSP00000505356.1:n.83-30C=
ENST00000303372.6:c.83-30C= ENSP00000304941.5:n.83-30C=
ENST00000426174.6:c.83-30C= ENSP00000395171.2:n.83-30C=
ENST00000541523.1:c.109-30C= ENSP00000437644.1:n.109-30C=
NM_001143850.2:c.83-30C= NP_001137322.1:n.83-30C=
NM_024809.4:c.83-30C= NP_079085.2:n.83-30C=
XM_005253623.2:c.83-30C= XP_005253680.1:n.83-30C=
XM_006719605.2:c.83-30C= XP_006719668.1:n.83-30C=
XM_006719605.3:c.83-30C= XP_006719668.1:n.83-30C=
XM_017019974.1:c.83-30C= XP_016875463.1:n.83-30C=
XM_017019975.1:c.-700-30C= XP_016875464.1:n.-700-30C=
NM_024809.5:c.83-30C= MANE Select NP_079085.2:n.83-30C=
NM_001143850.3:c.83-30C= NP_001137322.1:n.83-30C=