Canonical Allele Identifier: CA482266811

Gene: TCTN2

Linked Data

• MyVariant Identifiers: chr12:g.124171430C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123686883C>A , CM000674.2:g.123686883C>A	GRCh38
NC_000012.11:g.124171430C>A , CM000674.1:g.124171430C>A	GRCh37
NC_000012.10:g.122737383C>A	NCBI36
NG_030442.1:g.20771C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303372.7:c.612C>A MANE Select	ENSP00000304941.5:p.Thr204=
ENST00000679504.1:c.609C>A	ENSP00000505006.1:p.Thr203=
ENST00000680500.1:c.612C>A	ENSP00000506438.1:p.Thr204=
ENST00000680574.1:c.612C>A	ENSP00000505356.1:p.Thr204=
ENST00000303372.6:c.612C>A	ENSP00000304941.5:p.Thr204=
ENST00000426174.6:c.609C>A	ENSP00000395171.2:p.Thr203=
NM_001143850.2:c.609C>A	NP_001137322.1:p.Thr203=
NM_024809.4:c.612C>A	NP_079085.2:p.Thr204=
XM_005253623.2:c.612C>A	XP_005253680.1:p.Thr204=
XM_006719605.2:c.612C>A	XP_006719668.1:p.Thr204=
XM_006719605.3:c.612C>A	XP_006719668.1:p.Thr204=
XM_017019974.1:c.609C>A	XP_016875463.1:p.Thr203=
XM_017019975.1:c.-174C>A	XP_016875464.1:n.-174C>A
NM_024809.5:c.612C>A MANE Select	NP_079085.2:p.Thr204=
NM_001143850.3:c.609C>A	NP_001137322.1:p.Thr203=