Canonical Allele Identifier: CA471020951

Gene: TCTN3

Linked Data

• MyVariant Identifiers: chr10:g.97446282T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95686525T>C , CM000672.2:g.95686525T>C	GRCh38
NC_000010.10:g.97446282T>C , CM000672.1:g.97446282T>C	GRCh37
NC_000010.9:g.97436272T>C	NCBI36
NG_032953.1:g.12619A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371217.10:c.858A>G MANE Select	ENSP00000360261.5:p.Pro286=
ENST00000614499.5:c.912A>G	ENSP00000483364.2:p.Pro304=
ENST00000679485.1:n.882A>G
ENST00000679566.1:c.852+519A>G	ENSP00000505964.1:n.852+519A>G
ENST00000679984.1:c.*113A>G	ENSP00000504998.1:n.*113A>G
ENST00000680144.1:c.858A>G	ENSP00000506398.1:p.Pro286=
ENST00000680353.1:c.858A>G	ENSP00000505367.1:p.Pro286=
ENST00000680697.1:n.543-1901A>G
ENST00000680709.1:c.621A>G	ENSP00000505830.1:p.Pro207=
ENST00000681127.1:n.911A>G
ENST00000681739.1:n.913A>G
ENST00000681928.1:c.*130+519A>G	ENSP00000505552.1:n.*130+519A>G
ENST00000265993.13:c.912A>G	ENSP00000265993.9:p.Pro304=
ENST00000371209.5:c.858A>G	ENSP00000360253.5:p.Pro286=
ENST00000371217.9:c.858A>G	ENSP00000360261.5:p.Pro286=
ENST00000430368.6:c.621A>G	ENSP00000387567.1:p.Pro207=
ENST00000614499.4:c.858A>G	ENSP00000483364.1:p.Pro286=
NM_001143973.1:c.621A>G	NP_001137445.1:p.Pro207=
NM_015631.5:c.858A>G	NP_056446.4:p.Pro286=
XM_005269690.1:c.912A>G	XP_005269747.1:p.Pro304=
XM_011539627.1:c.912A>G	XP_011537929.1:p.Pro304=
XM_011539628.1:c.912A>G	XP_011537930.1:p.Pro304=
XM_005269690.2:c.912A>G	XP_005269747.1:p.Pro304=
XM_011539627.2:c.912A>G	XP_011537929.1:p.Pro304=
XM_011539628.2:c.912A>G	XP_011537930.1:p.Pro304=
XM_024447935.1:c.912A>G	XP_024303703.1:p.Pro304=
NM_015631.6:c.858A>G MANE Select	NP_056446.4:p.Pro286=
NM_001143973.2:c.621A>G	NP_001137445.1:p.Pro207=