Canonical Allele Identifier: CA377698735

Gene: TCTN3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95664117G>A , CM000672.2:g.95664117G>A	GRCh38
NC_000010.10:g.97423874G>A , CM000672.1:g.97423874G>A	GRCh37
NC_000010.9:g.97413864G>A	NCBI36
NG_032953.1:g.35027C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371217.10:c.1774C>T MANE Select	ENSP00000360261.5:p.Leu592Phe
ENST00000614499.5:c.1813C>T	ENSP00000483364.2:p.Leu605Phe
ENST00000679984.1:c.*1014C>T	ENSP00000504998.1:n.*1014C>T
ENST00000680144.1:c.1678C>T	ENSP00000506398.1:p.Leu560Phe
ENST00000680353.1:c.1525C>T	ENSP00000505367.1:p.Leu509Phe
ENST00000680697.1:n.1969C>T
ENST00000680709.1:c.1522C>T	ENSP00000505830.1:p.Leu508Phe
ENST00000680781.1:c.431C>T
ENST00000681185.1:n.476C>T
ENST00000681739.1:n.2155C>T
ENST00000681928.1:c.*314C>T	ENSP00000505552.1:n.*314C>T
ENST00000265993.13:c.1828C>T	ENSP00000265993.9:p.Leu610Phe
ENST00000371217.9:c.1774C>T	ENSP00000360261.5:p.Leu592Phe
ENST00000430368.6:c.1330C>T	ENSP00000387567.1:p.Leu444Phe
ENST00000614499.4:c.1774C>T	ENSP00000483364.1:p.Leu592Phe
NM_001143973.1:c.1330C>T	NP_001137445.1:p.Leu444Phe
NM_015631.5:c.1774C>T	NP_056446.4:p.Leu592Phe
XM_005269690.1:c.1747C>T	XP_005269747.1:p.Leu583Phe
XM_011539627.1:c.1813C>T	XP_011537929.1:p.Leu605Phe
XM_011539628.1:c.1690C>T	XP_011537930.1:p.Leu564Phe
XM_005269690.2:c.1747C>T	XP_005269747.1:p.Leu583Phe
XM_011539627.2:c.1813C>T	XP_011537929.1:p.Leu605Phe
XM_011539628.2:c.1690C>T	XP_011537930.1:p.Leu564Phe
XM_024447935.1:c.1732C>T	XP_024303703.1:p.Leu578Phe
NM_015631.6:c.1774C>T MANE Select	NP_056446.4:p.Leu592Phe
NM_001143973.2:c.1330C>T	NP_001137445.1:p.Leu444Phe