Canonical Allele Identifier: CA377706447

Gene: TCTN3

Linked Data

• MyVariant Identifiers: chr10:g.97446284G>A (hg19) ; chr10:g.95686527G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95686527G>A , CM000672.2:g.95686527G>A	GRCh38
NC_000010.10:g.97446284G>A , CM000672.1:g.97446284G>A	GRCh37
NC_000010.9:g.97436274G>A	NCBI36
NG_032953.1:g.12617C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371217.10:c.856C>T MANE Select	ENSP00000360261.5:p.Pro286Ser
ENST00000614499.5:c.910C>T	ENSP00000483364.2:p.Pro304Ser
ENST00000679485.1:n.880C>T
ENST00000679566.1:c.852+517C>T	ENSP00000505964.1:n.852+517C>T
ENST00000679984.1:c.*111C>T	ENSP00000504998.1:n.*111C>T
ENST00000680144.1:c.856C>T	ENSP00000506398.1:p.Pro286Ser
ENST00000680353.1:c.856C>T	ENSP00000505367.1:p.Pro286Ser
ENST00000680697.1:n.543-1903C>T
ENST00000680709.1:c.619C>T	ENSP00000505830.1:p.Pro207Ser
ENST00000681127.1:n.909C>T
ENST00000681739.1:n.911C>T
ENST00000681928.1:c.*130+517C>T	ENSP00000505552.1:n.*130+517C>T
ENST00000265993.13:c.910C>T	ENSP00000265993.9:p.Pro304Ser
ENST00000371209.5:c.856C>T	ENSP00000360253.5:p.Pro286Ser
ENST00000371217.9:c.856C>T	ENSP00000360261.5:p.Pro286Ser
ENST00000430368.6:c.619C>T	ENSP00000387567.1:p.Pro207Ser
ENST00000614499.4:c.856C>T	ENSP00000483364.1:p.Pro286Ser
NM_001143973.1:c.619C>T	NP_001137445.1:p.Pro207Ser
NM_015631.5:c.856C>T	NP_056446.4:p.Pro286Ser
XM_005269690.1:c.910C>T	XP_005269747.1:p.Pro304Ser
XM_011539627.1:c.910C>T	XP_011537929.1:p.Pro304Ser
XM_011539628.1:c.910C>T	XP_011537930.1:p.Pro304Ser
XM_005269690.2:c.910C>T	XP_005269747.1:p.Pro304Ser
XM_011539627.2:c.910C>T	XP_011537929.1:p.Pro304Ser
XM_011539628.2:c.910C>T	XP_011537930.1:p.Pro304Ser
XM_024447935.1:c.910C>T	XP_024303703.1:p.Pro304Ser
NM_015631.6:c.856C>T MANE Select	NP_056446.4:p.Pro286Ser
NM_001143973.2:c.619C>T	NP_001137445.1:p.Pro207Ser