Canonical Allele Identifier: CA377698759

Gene: TCTN3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95664129C>T , CM000672.2:g.95664129C>T	GRCh38
NC_000010.10:g.97423886C>T , CM000672.1:g.97423886C>T	GRCh37
NC_000010.9:g.97413876C>T	NCBI36
NG_032953.1:g.35015G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371217.10:c.1762G>A MANE Select	ENSP00000360261.5:p.Val588Ile
ENST00000614499.5:c.1801G>A	ENSP00000483364.2:p.Val601Ile
ENST00000679984.1:c.*1002G>A	ENSP00000504998.1:n.*1002G>A
ENST00000680144.1:c.1666G>A	ENSP00000506398.1:p.Val556Ile
ENST00000680353.1:c.1513G>A	ENSP00000505367.1:p.Val505Ile
ENST00000680697.1:n.1957G>A
ENST00000680709.1:c.1510G>A	ENSP00000505830.1:p.Val504Ile
ENST00000680781.1:c.419G>A
ENST00000681185.1:n.464G>A
ENST00000681739.1:n.2143G>A
ENST00000681928.1:c.*302G>A	ENSP00000505552.1:n.*302G>A
ENST00000265993.13:c.1816G>A	ENSP00000265993.9:p.Val606Ile
ENST00000371217.9:c.1762G>A	ENSP00000360261.5:p.Val588Ile
ENST00000430368.6:c.1318G>A	ENSP00000387567.1:p.Val440Ile
ENST00000614499.4:c.1762G>A	ENSP00000483364.1:p.Val588Ile
NM_001143973.1:c.1318G>A	NP_001137445.1:p.Val440Ile
NM_015631.5:c.1762G>A	NP_056446.4:p.Val588Ile
XM_005269690.1:c.1735G>A	XP_005269747.1:p.Val579Ile
XM_011539627.1:c.1801G>A	XP_011537929.1:p.Val601Ile
XM_011539628.1:c.1678G>A	XP_011537930.1:p.Val560Ile
XM_005269690.2:c.1735G>A	XP_005269747.1:p.Val579Ile
XM_011539627.2:c.1801G>A	XP_011537929.1:p.Val601Ile
XM_011539628.2:c.1678G>A	XP_011537930.1:p.Val560Ile
XM_024447935.1:c.1720G>A	XP_024303703.1:p.Val574Ile
NM_015631.6:c.1762G>A MANE Select	NP_056446.4:p.Val588Ile
NM_001143973.2:c.1318G>A	NP_001137445.1:p.Val440Ile