Canonical Allele Identifier: CA595349623

Gene: TCTN3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95682808T>C , CM000672.2:g.95682808T>C	GRCh38
NC_000010.10:g.97442565T>C , CM000672.1:g.97442565T>C	GRCh37
NC_000010.9:g.97432555T>C	NCBI36
NG_032953.1:g.16336A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371217.10:c.1299-4A>G MANE Select	ENSP00000360261.5:n.1299-4A>G
ENST00000614499.5:c.1338-4A>G	ENSP00000483364.2:n.1338-4A>G
ENST00000679485.1:n.1323-4A>G
ENST00000679984.1:c.*539-4A>G	ENSP00000504998.1:n.*539-4A>G
ENST00000680144.1:c.1203-4A>G	ENSP00000506398.1:n.1203-4A>G
ENST00000680353.1:c.1203+714A>G	ENSP00000505367.1:n.1203+714A>G
ENST00000680697.1:n.1490A>G
ENST00000680709.1:c.1047-4A>G	ENSP00000505830.1:n.1047-4A>G
ENST00000681739.1:n.1680-4A>G
ENST00000681928.1:c.*130+4236A>G	ENSP00000505552.1:n.*130+4236A>G
ENST00000265993.13:c.1353-4A>G	ENSP00000265993.9:n.1353-4A>G
ENST00000371217.9:c.1299-4A>G	ENSP00000360261.5:n.1299-4A>G
ENST00000430368.6:c.855-4A>G	ENSP00000387567.1:n.855-4A>G
ENST00000614499.4:c.1299-4A>G	ENSP00000483364.1:n.1299-4A>G
NM_001143973.1:c.855-4A>G	NP_001137445.1:n.855-4A>G
NM_015631.5:c.1299-4A>G	NP_056446.4:n.1299-4A>G
XM_005269690.1:c.1272-4A>G	XP_005269747.1:n.1272-4A>G
XM_011539627.1:c.1338-4A>G	XP_011537929.1:n.1338-4A>G
XM_011539628.1:c.1353-4A>G	XP_011537930.1:n.1353-4A>G
XM_005269690.2:c.1272-4A>G	XP_005269747.1:n.1272-4A>G
XM_011539627.2:c.1338-4A>G	XP_011537929.1:n.1338-4A>G
XM_011539628.2:c.1353-4A>G	XP_011537930.1:n.1353-4A>G
XM_024447935.1:c.1257-4A>G	XP_024303703.1:n.1257-4A>G
NM_015631.6:c.1299-4A>G MANE Select	NP_056446.4:n.1299-4A>G
NM_001143973.2:c.855-4A>G	NP_001137445.1:n.855-4A>G