Canonical Allele Identifier: CA377706409

Gene: TCTN3

Linked Data

• MyVariant Identifiers: chr10:g.97446277C>T (hg19) ; chr10:g.95686520C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95686520C>T , CM000672.2:g.95686520C>T	GRCh38
NC_000010.10:g.97446277C>T , CM000672.1:g.97446277C>T	GRCh37
NC_000010.9:g.97436267C>T	NCBI36
NG_032953.1:g.12624G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371217.10:c.863G>A MANE Select	ENSP00000360261.5:p.Ser288Asn
ENST00000614499.5:c.917G>A	ENSP00000483364.2:p.Ser306Asn
ENST00000679485.1:n.887G>A
ENST00000679566.1:c.852+524G>A	ENSP00000505964.1:n.852+524G>A
ENST00000679984.1:c.*118G>A	ENSP00000504998.1:n.*118G>A
ENST00000680144.1:c.863G>A	ENSP00000506398.1:p.Ser288Asn
ENST00000680353.1:c.863G>A	ENSP00000505367.1:p.Ser288Asn
ENST00000680697.1:n.543-1896G>A
ENST00000680709.1:c.626G>A	ENSP00000505830.1:p.Ser209Asn
ENST00000681127.1:n.916G>A
ENST00000681739.1:n.918G>A
ENST00000681928.1:c.*130+524G>A	ENSP00000505552.1:n.*130+524G>A
ENST00000265993.13:c.917G>A	ENSP00000265993.9:p.Ser306Asn
ENST00000371209.5:c.863G>A	ENSP00000360253.5:p.Ser288Asn
ENST00000371217.9:c.863G>A	ENSP00000360261.5:p.Ser288Asn
ENST00000430368.6:c.626G>A	ENSP00000387567.1:p.Ser209Asn
ENST00000614499.4:c.863G>A	ENSP00000483364.1:p.Ser288Asn
NM_001143973.1:c.626G>A	NP_001137445.1:p.Ser209Asn
NM_015631.5:c.863G>A	NP_056446.4:p.Ser288Asn
XM_005269690.1:c.917G>A	XP_005269747.1:p.Ser306Asn
XM_011539627.1:c.917G>A	XP_011537929.1:p.Ser306Asn
XM_011539628.1:c.917G>A	XP_011537930.1:p.Ser306Asn
XM_005269690.2:c.917G>A	XP_005269747.1:p.Ser306Asn
XM_011539627.2:c.917G>A	XP_011537929.1:p.Ser306Asn
XM_011539628.2:c.917G>A	XP_011537930.1:p.Ser306Asn
XM_024447935.1:c.917G>A	XP_024303703.1:p.Ser306Asn
NM_015631.6:c.863G>A MANE Select	NP_056446.4:p.Ser288Asn
NM_001143973.2:c.626G>A	NP_001137445.1:p.Ser209Asn