Canonical Allele Identifier: CA595349962

Gene: TCTN3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95686492T>A , CM000672.2:g.95686492T>A	GRCh38
NC_000010.10:g.97446249T>A , CM000672.1:g.97446249T>A	GRCh37
NC_000010.9:g.97436239T>A	NCBI36
NG_032953.1:g.12652A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371217.10:c.888+3A>T MANE Select	ENSP00000360261.5:n.888+3A>T
ENST00000614499.5:c.942+3A>T	ENSP00000483364.2:n.942+3A>T
ENST00000679485.1:n.912+3A>T
ENST00000679566.1:c.852+552A>T	ENSP00000505964.1:n.852+552A>T
ENST00000679984.1:c.*143+3A>T	ENSP00000504998.1:n.*143+3A>T
ENST00000680144.1:c.888+3A>T	ENSP00000506398.1:n.888+3A>T
ENST00000680353.1:c.888+3A>T	ENSP00000505367.1:n.888+3A>T
ENST00000680697.1:n.543-1868A>T
ENST00000680709.1:c.651+3A>T	ENSP00000505830.1:n.651+3A>T
ENST00000681127.1:n.944A>T
ENST00000681739.1:n.943+3A>T
ENST00000681928.1:c.*130+552A>T	ENSP00000505552.1:n.*130+552A>T
ENST00000265993.13:c.942+3A>T	ENSP00000265993.9:n.942+3A>T
ENST00000371209.5:c.888+3A>T	ENSP00000360253.5:n.888+3A>T
ENST00000371217.9:c.888+3A>T	ENSP00000360261.5:n.888+3A>T
ENST00000430368.6:c.651+3A>T	ENSP00000387567.1:n.651+3A>T
ENST00000614499.4:c.888+3A>T	ENSP00000483364.1:n.888+3A>T
NM_001143973.1:c.651+3A>T	NP_001137445.1:n.651+3A>T
NM_015631.5:c.888+3A>T	NP_056446.4:n.888+3A>T
XM_005269690.1:c.942+3A>T	XP_005269747.1:n.942+3A>T
XM_011539627.1:c.942+3A>T	XP_011537929.1:n.942+3A>T
XM_011539628.1:c.942+3A>T	XP_011537930.1:n.942+3A>T
XM_005269690.2:c.942+3A>T	XP_005269747.1:n.942+3A>T
XM_011539627.2:c.942+3A>T	XP_011537929.1:n.942+3A>T
XM_011539628.2:c.942+3A>T	XP_011537930.1:n.942+3A>T
XM_024447935.1:c.942+3A>T	XP_024303703.1:n.942+3A>T
NM_015631.6:c.888+3A>T MANE Select	NP_056446.4:n.888+3A>T
NM_001143973.2:c.651+3A>T	NP_001137445.1:n.651+3A>T