Canonical Allele Identifier: CA2621689119

Gene: TCTN2

Linked Data

• gnomAD v4: 12-123686784-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123686784C>A , CM000674.2:g.123686784C>A	GRCh38
NC_000012.11:g.124171331C>A , CM000674.1:g.124171331C>A	GRCh37
NC_000012.10:g.122737284C>A	NCBI36
NG_030442.1:g.20672C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303372.7:c.565-52C>A MANE Select	ENSP00000304941.5:n.565-52C>A
ENST00000679504.1:c.562-52C>A	ENSP00000505006.1:n.562-52C>A
ENST00000680500.1:c.565-52C>A	ENSP00000506438.1:n.565-52C>A
ENST00000680574.1:c.565-52C>A	ENSP00000505356.1:n.565-52C>A
ENST00000303372.6:c.565-52C>A	ENSP00000304941.5:n.565-52C>A
ENST00000426174.6:c.562-52C>A	ENSP00000395171.2:n.562-52C>A
NM_001143850.2:c.562-52C>A	NP_001137322.1:n.562-52C>A
NM_024809.4:c.565-52C>A	NP_079085.2:n.565-52C>A
XM_005253623.2:c.565-52C>A	XP_005253680.1:n.565-52C>A
XM_006719605.2:c.565-52C>A	XP_006719668.1:n.565-52C>A
XM_006719605.3:c.565-52C>A	XP_006719668.1:n.565-52C>A
XM_017019974.1:c.562-52C>A	XP_016875463.1:n.562-52C>A
XM_017019975.1:c.-221-52C>A	XP_016875464.1:n.-221-52C>A
NM_024809.5:c.565-52C>A MANE Select	NP_079085.2:n.565-52C>A
NM_001143850.3:c.562-52C>A	NP_001137322.1:n.562-52C>A