Canonical Allele Identifier: CA2621687396

Gene: TCTN2

Linked Data

• gnomAD v4: 12-123671408-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123671408C>G , CM000674.2:g.123671408C>G	GRCh38
NC_000012.11:g.124155955C>G , CM000674.1:g.124155955C>G	GRCh37
NC_000012.10:g.122721908C>G	NCBI36
NG_030442.1:g.5296C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303372.7:c.82+86C>G MANE Select	ENSP00000304941.5:n.82+86C>G
ENST00000679504.1:c.82+86C>G	ENSP00000505006.1:n.82+86C>G
ENST00000680500.1:c.82+86C>G	ENSP00000506438.1:n.82+86C>G
ENST00000680574.1:c.82+86C>G	ENSP00000505356.1:n.82+86C>G
ENST00000303372.6:c.82+86C>G	ENSP00000304941.5:n.82+86C>G
ENST00000426174.6:c.82+86C>G	ENSP00000395171.2:n.82+86C>G
ENST00000541523.1:c.108+60C>G	ENSP00000437644.1:n.108+60C>G
NM_001143850.2:c.82+86C>G	NP_001137322.1:n.82+86C>G
NM_024809.4:c.82+86C>G	NP_079085.2:n.82+86C>G
XM_005253623.2:c.82+86C>G	XP_005253680.1:n.82+86C>G
XM_006719605.2:c.82+86C>G	XP_006719668.1:n.82+86C>G
XM_006719605.3:c.82+86C>G	XP_006719668.1:n.82+86C>G
XM_017019974.1:c.82+86C>G	XP_016875463.1:n.82+86C>G
XM_017019975.1:c.-701+86C>G	XP_016875464.1:n.-701+86C>G
NM_024809.5:c.82+86C>G MANE Select	NP_079085.2:n.82+86C>G
NM_001143850.3:c.82+86C>G	NP_001137322.1:n.82+86C>G