Canonical Allele Identifier: CA5620852

Gene: TCTN3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95682722T>C , CM000672.2:g.95682722T>C	GRCh38
NC_000010.10:g.97442479T>C , CM000672.1:g.97442479T>C	GRCh37
NC_000010.9:g.97432469T>C	NCBI36
NG_032953.1:g.16422A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371217.10:c.1381A>G MANE Select	ENSP00000360261.5:p.Ile461Val
ENST00000614499.5:c.1420A>G	ENSP00000483364.2:p.Ile474Val
ENST00000679485.1:n.1405A>G
ENST00000679984.1:c.*621A>G	ENSP00000504998.1:n.*621A>G
ENST00000680144.1:c.1285A>G	ENSP00000506398.1:p.Ile429Val
ENST00000680353.1:c.1203+800A>G	ENSP00000505367.1:n.1203+800A>G
ENST00000680697.1:n.1576A>G
ENST00000680709.1:c.1129A>G	ENSP00000505830.1:p.Ile377Val
ENST00000681739.1:n.1762A>G
ENST00000681928.1:c.*130+4322A>G	ENSP00000505552.1:n.*130+4322A>G
ENST00000265993.13:c.1435A>G	ENSP00000265993.9:p.Ile479Val
ENST00000371217.9:c.1381A>G	ENSP00000360261.5:p.Ile461Val
ENST00000430368.6:c.937A>G	ENSP00000387567.1:p.Ile313Val
ENST00000614499.4:c.1381A>G	ENSP00000483364.1:p.Ile461Val
NM_001143973.1:c.937A>G	NP_001137445.1:p.Ile313Val
NM_015631.5:c.1381A>G	NP_056446.4:p.Ile461Val
XM_005269690.1:c.1354A>G	XP_005269747.1:p.Ile452Val
XM_011539627.1:c.1420A>G	XP_011537929.1:p.Ile474Val
XM_011539628.1:c.1435A>G	XP_011537930.1:p.Ile479Val
XM_005269690.2:c.1354A>G	XP_005269747.1:p.Ile452Val
XM_011539627.2:c.1420A>G	XP_011537929.1:p.Ile474Val
XM_011539628.2:c.1435A>G	XP_011537930.1:p.Ile479Val
XM_024447935.1:c.1339A>G	XP_024303703.1:p.Ile447Val
NM_015631.6:c.1381A>G MANE Select	NP_056446.4:p.Ile461Val
NM_001143973.2:c.937A>G	NP_001137445.1:p.Ile313Val