Canonical Allele Identifier: CA471248132

Gene: TCTN3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95664112G>T , CM000672.2:g.95664112G>T	GRCh38
NC_000010.10:g.97423869G>T , CM000672.1:g.97423869G>T	GRCh37
NC_000010.9:g.97413859G>T	NCBI36
NG_032953.1:g.35032C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371217.10:c.1779C>A MANE Select	ENSP00000360261.5:p.Ile593=
ENST00000614499.5:c.1818C>A	ENSP00000483364.2:p.Ile606=
ENST00000679984.1:c.*1019C>A	ENSP00000504998.1:n.*1019C>A
ENST00000680144.1:c.1683C>A	ENSP00000506398.1:p.Ile561=
ENST00000680353.1:c.1530C>A	ENSP00000505367.1:p.Ile510=
ENST00000680697.1:n.1974C>A
ENST00000680709.1:c.1527C>A	ENSP00000505830.1:p.Ile509=
ENST00000680781.1:c.436C>A
ENST00000681185.1:n.481C>A
ENST00000681739.1:n.2160C>A
ENST00000681928.1:c.*319C>A	ENSP00000505552.1:n.*319C>A
ENST00000265993.13:c.1833C>A	ENSP00000265993.9:p.Ile611=
ENST00000371217.9:c.1779C>A	ENSP00000360261.5:p.Ile593=
ENST00000430368.6:c.1335C>A	ENSP00000387567.1:p.Ile445=
ENST00000614499.4:c.1779C>A	ENSP00000483364.1:p.Ile593=
NM_001143973.1:c.1335C>A	NP_001137445.1:p.Ile445=
NM_015631.5:c.1779C>A	NP_056446.4:p.Ile593=
XM_005269690.1:c.1752C>A	XP_005269747.1:p.Ile584=
XM_011539627.1:c.1818C>A	XP_011537929.1:p.Ile606=
XM_011539628.1:c.1695C>A	XP_011537930.1:p.Ile565=
XM_005269690.2:c.1752C>A	XP_005269747.1:p.Ile584=
XM_011539627.2:c.1818C>A	XP_011537929.1:p.Ile606=
XM_011539628.2:c.1695C>A	XP_011537930.1:p.Ile565=
XM_024447935.1:c.1737C>A	XP_024303703.1:p.Ile579=
NM_015631.6:c.1779C>A MANE Select	NP_056446.4:p.Ile593=
NM_001143973.2:c.1335C>A	NP_001137445.1:p.Ile445=