Canonical Allele Identifier: CA471019201

Gene: TCTN3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95682750A>G , CM000672.2:g.95682750A>G	GRCh38
NC_000010.10:g.97442507A>G , CM000672.1:g.97442507A>G	GRCh37
NC_000010.9:g.97432497A>G	NCBI36
NG_032953.1:g.16394T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371217.10:c.1353T>C MANE Select	ENSP00000360261.5:p.His451=
ENST00000614499.5:c.1392T>C	ENSP00000483364.2:p.His464=
ENST00000679485.1:n.1377T>C
ENST00000679984.1:c.*593T>C	ENSP00000504998.1:n.*593T>C
ENST00000680144.1:c.1257T>C	ENSP00000506398.1:p.His419=
ENST00000680353.1:c.1203+772T>C	ENSP00000505367.1:n.1203+772T>C
ENST00000680697.1:n.1548T>C
ENST00000680709.1:c.1101T>C	ENSP00000505830.1:p.His367=
ENST00000681739.1:n.1734T>C
ENST00000681928.1:c.*130+4294T>C	ENSP00000505552.1:n.*130+4294T>C
ENST00000265993.13:c.1407T>C	ENSP00000265993.9:p.His469=
ENST00000371217.9:c.1353T>C	ENSP00000360261.5:p.His451=
ENST00000430368.6:c.909T>C	ENSP00000387567.1:p.His303=
ENST00000614499.4:c.1353T>C	ENSP00000483364.1:p.His451=
NM_001143973.1:c.909T>C	NP_001137445.1:p.His303=
NM_015631.5:c.1353T>C	NP_056446.4:p.His451=
XM_005269690.1:c.1326T>C	XP_005269747.1:p.His442=
XM_011539627.1:c.1392T>C	XP_011537929.1:p.His464=
XM_011539628.1:c.1407T>C	XP_011537930.1:p.His469=
XM_005269690.2:c.1326T>C	XP_005269747.1:p.His442=
XM_011539627.2:c.1392T>C	XP_011537929.1:p.His464=
XM_011539628.2:c.1407T>C	XP_011537930.1:p.His469=
XM_024447935.1:c.1311T>C	XP_024303703.1:p.His437=
NM_015631.6:c.1353T>C MANE Select	NP_056446.4:p.His451=
NM_001143973.2:c.909T>C	NP_001137445.1:p.His303=