Canonical Allele Identifier: CA5620748

Gene: TCTN3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95664136T>A , CM000672.2:g.95664136T>A	GRCh38
NC_000010.10:g.97423893T>A , CM000672.1:g.97423893T>A	GRCh37
NC_000010.9:g.97413883T>A	NCBI36
NG_032953.1:g.35008A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371217.10:c.1755A>T MANE Select	ENSP00000360261.5:p.Lys585Asn
ENST00000614499.5:c.1794A>T	ENSP00000483364.2:p.Lys598Asn
ENST00000679984.1:c.*995A>T	ENSP00000504998.1:n.*995A>T
ENST00000680144.1:c.1659A>T	ENSP00000506398.1:p.Lys553Asn
ENST00000680353.1:c.1506A>T	ENSP00000505367.1:p.Lys502Asn
ENST00000680697.1:n.1950A>T
ENST00000680709.1:c.1503A>T	ENSP00000505830.1:p.Lys501Asn
ENST00000680781.1:c.412A>T
ENST00000681185.1:n.457A>T
ENST00000681739.1:n.2136A>T
ENST00000681928.1:c.*295A>T	ENSP00000505552.1:n.*295A>T
ENST00000265993.13:c.1809A>T	ENSP00000265993.9:p.Lys603Asn
ENST00000371217.9:c.1755A>T	ENSP00000360261.5:p.Lys585Asn
ENST00000430368.6:c.1311A>T	ENSP00000387567.1:p.Lys437Asn
ENST00000614499.4:c.1755A>T	ENSP00000483364.1:p.Lys585Asn
NM_001143973.1:c.1311A>T	NP_001137445.1:p.Lys437Asn
NM_015631.5:c.1755A>T	NP_056446.4:p.Lys585Asn
XM_005269690.1:c.1728A>T	XP_005269747.1:p.Lys576Asn
XM_011539627.1:c.1794A>T	XP_011537929.1:p.Lys598Asn
XM_011539628.1:c.1671A>T	XP_011537930.1:p.Lys557Asn
XM_005269690.2:c.1728A>T	XP_005269747.1:p.Lys576Asn
XM_011539627.2:c.1794A>T	XP_011537929.1:p.Lys598Asn
XM_011539628.2:c.1671A>T	XP_011537930.1:p.Lys557Asn
XM_024447935.1:c.1713A>T	XP_024303703.1:p.Lys571Asn
NM_015631.6:c.1755A>T MANE Select	NP_056446.4:p.Lys585Asn
NM_001143973.2:c.1311A>T	NP_001137445.1:p.Lys437Asn