Canonical Allele Identifier: CA5620844

Gene: TCTN3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95682665G>A , CM000672.2:g.95682665G>A	GRCh38
NC_000010.10:g.97442422G>A , CM000672.1:g.97442422G>A	GRCh37
NC_000010.9:g.97432412G>A	NCBI36
NG_032953.1:g.16479C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371217.10:c.1438C>T MANE Select	ENSP00000360261.5:p.His480Tyr
ENST00000614499.5:c.1477C>T	ENSP00000483364.2:p.His493Tyr
ENST00000679485.1:n.1462C>T
ENST00000679984.1:c.*678C>T	ENSP00000504998.1:n.*678C>T
ENST00000680144.1:c.1342C>T	ENSP00000506398.1:p.His448Tyr
ENST00000680353.1:c.1203+857C>T	ENSP00000505367.1:n.1203+857C>T
ENST00000680697.1:n.1633C>T
ENST00000680709.1:c.1186C>T	ENSP00000505830.1:p.His396Tyr
ENST00000681739.1:n.1819C>T
ENST00000681928.1:c.*130+4379C>T	ENSP00000505552.1:n.*130+4379C>T
ENST00000265993.13:c.1492C>T	ENSP00000265993.9:p.His498Tyr
ENST00000371217.9:c.1438C>T	ENSP00000360261.5:p.His480Tyr
ENST00000430368.6:c.994C>T	ENSP00000387567.1:p.His332Tyr
ENST00000614499.4:c.1438C>T	ENSP00000483364.1:p.His480Tyr
NM_001143973.1:c.994C>T	NP_001137445.1:p.His332Tyr
NM_015631.5:c.1438C>T	NP_056446.4:p.His480Tyr
XM_005269690.1:c.1411C>T	XP_005269747.1:p.His471Tyr
XM_011539627.1:c.1477C>T	XP_011537929.1:p.His493Tyr
XM_011539628.1:c.1492C>T	XP_011537930.1:p.His498Tyr
XM_005269690.2:c.1411C>T	XP_005269747.1:p.His471Tyr
XM_011539627.2:c.1477C>T	XP_011537929.1:p.His493Tyr
XM_011539628.2:c.1492C>T	XP_011537930.1:p.His498Tyr
XM_024447935.1:c.1396C>T	XP_024303703.1:p.His466Tyr
NM_015631.6:c.1438C>T MANE Select	NP_056446.4:p.His480Tyr
NM_001143973.2:c.994C>T	NP_001137445.1:p.His332Tyr