Canonical Allele Identifier: CA377706431

Gene: TCTN3

Linked Data

• MyVariant Identifiers: chr10:g.97446280C>A (hg19) ; chr10:g.95686523C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95686523C>A , CM000672.2:g.95686523C>A	GRCh38
NC_000010.10:g.97446280C>A , CM000672.1:g.97446280C>A	GRCh37
NC_000010.9:g.97436270C>A	NCBI36
NG_032953.1:g.12621G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371217.10:c.860G>T MANE Select	ENSP00000360261.5:p.Arg287Ile
ENST00000614499.5:c.914G>T	ENSP00000483364.2:p.Arg305Ile
ENST00000679485.1:n.884G>T
ENST00000679566.1:c.852+521G>T	ENSP00000505964.1:n.852+521G>T
ENST00000679984.1:c.*115G>T	ENSP00000504998.1:n.*115G>T
ENST00000680144.1:c.860G>T	ENSP00000506398.1:p.Arg287Ile
ENST00000680353.1:c.860G>T	ENSP00000505367.1:p.Arg287Ile
ENST00000680697.1:n.543-1899G>T
ENST00000680709.1:c.623G>T	ENSP00000505830.1:p.Arg208Ile
ENST00000681127.1:n.913G>T
ENST00000681739.1:n.915G>T
ENST00000681928.1:c.*130+521G>T	ENSP00000505552.1:n.*130+521G>T
ENST00000265993.13:c.914G>T	ENSP00000265993.9:p.Arg305Ile
ENST00000371209.5:c.860G>T	ENSP00000360253.5:p.Arg287Ile
ENST00000371217.9:c.860G>T	ENSP00000360261.5:p.Arg287Ile
ENST00000430368.6:c.623G>T	ENSP00000387567.1:p.Arg208Ile
ENST00000614499.4:c.860G>T	ENSP00000483364.1:p.Arg287Ile
NM_001143973.1:c.623G>T	NP_001137445.1:p.Arg208Ile
NM_015631.5:c.860G>T	NP_056446.4:p.Arg287Ile
XM_005269690.1:c.914G>T	XP_005269747.1:p.Arg305Ile
XM_011539627.1:c.914G>T	XP_011537929.1:p.Arg305Ile
XM_011539628.1:c.914G>T	XP_011537930.1:p.Arg305Ile
XM_005269690.2:c.914G>T	XP_005269747.1:p.Arg305Ile
XM_011539627.2:c.914G>T	XP_011537929.1:p.Arg305Ile
XM_011539628.2:c.914G>T	XP_011537930.1:p.Arg305Ile
XM_024447935.1:c.914G>T	XP_024303703.1:p.Arg305Ile
NM_015631.6:c.860G>T MANE Select	NP_056446.4:p.Arg287Ile
NM_001143973.2:c.623G>T	NP_001137445.1:p.Arg208Ile