Canonical Allele Identifier: CA5620981

Gene: TCTN3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95684586G>T , CM000672.2:g.95684586G>T	GRCh38
NC_000010.10:g.97444343G>T , CM000672.1:g.97444343G>T	GRCh37
NC_000010.9:g.97434333G>T	NCBI36
NG_032953.1:g.14558C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371217.10:c.1008C>A MANE Select	ENSP00000360261.5:p.Ile336=
ENST00000614499.5:c.1062C>A	ENSP00000483364.2:p.Ile354=
ENST00000679485.1:n.1032C>A
ENST00000679566.1:c.891C>A	ENSP00000505964.1:p.Ile297=
ENST00000679984.1:c.*263C>A	ENSP00000504998.1:n.*263C>A
ENST00000680144.1:c.927C>A	ENSP00000506398.1:p.Ile309=
ENST00000680353.1:c.1008C>A	ENSP00000505367.1:p.Ile336=
ENST00000680697.1:n.581C>A
ENST00000680709.1:c.771C>A	ENSP00000505830.1:p.Ile257=
ENST00000681127.1:n.2850C>A
ENST00000681739.1:n.1063C>A
ENST00000681928.1:c.*130+2458C>A	ENSP00000505552.1:n.*130+2458C>A
ENST00000265993.13:c.1062C>A	ENSP00000265993.9:p.Ile354=
ENST00000371209.5:c.1008C>A	ENSP00000360253.5:p.Ile336=
ENST00000371217.9:c.1008C>A	ENSP00000360261.5:p.Ile336=
ENST00000430368.6:c.652-957C>A	ENSP00000387567.1:n.652-957C>A
ENST00000614499.4:c.1008C>A	ENSP00000483364.1:p.Ile336=
NM_001143973.1:c.652-957C>A	NP_001137445.1:n.652-957C>A
NM_015631.5:c.1008C>A	NP_056446.4:p.Ile336=
XM_005269690.1:c.981C>A	XP_005269747.1:p.Ile327=
XM_011539627.1:c.1062C>A	XP_011537929.1:p.Ile354=
XM_011539628.1:c.1062C>A	XP_011537930.1:p.Ile354=
XM_005269690.2:c.981C>A	XP_005269747.1:p.Ile327=
XM_011539627.2:c.1062C>A	XP_011537929.1:p.Ile354=
XM_011539628.2:c.1062C>A	XP_011537930.1:p.Ile354=
XM_024447935.1:c.981C>A	XP_024303703.1:p.Ile327=
NM_015631.6:c.1008C>A MANE Select	NP_056446.4:p.Ile336=
NM_001143973.2:c.652-957C>A	NP_001137445.1:n.652-957C>A