Canonical Allele Identifier: CA471020947

Gene: TCTN3

Linked Data

• MyVariant Identifiers: chr10:g.97446281T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95686524T>G , CM000672.2:g.95686524T>G	GRCh38
NC_000010.10:g.97446281T>G , CM000672.1:g.97446281T>G	GRCh37
NC_000010.9:g.97436271T>G	NCBI36
NG_032953.1:g.12620A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371217.10:c.859A>C MANE Select	ENSP00000360261.5:p.Arg287=
ENST00000614499.5:c.913A>C	ENSP00000483364.2:p.Arg305=
ENST00000679485.1:n.883A>C
ENST00000679566.1:c.852+520A>C	ENSP00000505964.1:n.852+520A>C
ENST00000679984.1:c.*114A>C	ENSP00000504998.1:n.*114A>C
ENST00000680144.1:c.859A>C	ENSP00000506398.1:p.Arg287=
ENST00000680353.1:c.859A>C	ENSP00000505367.1:p.Arg287=
ENST00000680697.1:n.543-1900A>C
ENST00000680709.1:c.622A>C	ENSP00000505830.1:p.Arg208=
ENST00000681127.1:n.912A>C
ENST00000681739.1:n.914A>C
ENST00000681928.1:c.*130+520A>C	ENSP00000505552.1:n.*130+520A>C
ENST00000265993.13:c.913A>C	ENSP00000265993.9:p.Arg305=
ENST00000371209.5:c.859A>C	ENSP00000360253.5:p.Arg287=
ENST00000371217.9:c.859A>C	ENSP00000360261.5:p.Arg287=
ENST00000430368.6:c.622A>C	ENSP00000387567.1:p.Arg208=
ENST00000614499.4:c.859A>C	ENSP00000483364.1:p.Arg287=
NM_001143973.1:c.622A>C	NP_001137445.1:p.Arg208=
NM_015631.5:c.859A>C	NP_056446.4:p.Arg287=
XM_005269690.1:c.913A>C	XP_005269747.1:p.Arg305=
XM_011539627.1:c.913A>C	XP_011537929.1:p.Arg305=
XM_011539628.1:c.913A>C	XP_011537930.1:p.Arg305=
XM_005269690.2:c.913A>C	XP_005269747.1:p.Arg305=
XM_011539627.2:c.913A>C	XP_011537929.1:p.Arg305=
XM_011539628.2:c.913A>C	XP_011537930.1:p.Arg305=
XM_024447935.1:c.913A>C	XP_024303703.1:p.Arg305=
NM_015631.6:c.859A>C MANE Select	NP_056446.4:p.Arg287=
NM_001143973.2:c.622A>C	NP_001137445.1:p.Arg208=