Canonical Allele Identifier: CA377714661

Gene: TCTN3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95693899T>C , CM000672.2:g.95693899T>C	GRCh38
NC_000010.10:g.97453656T>C , CM000672.1:g.97453656T>C	GRCh37
NC_000010.9:g.97443646T>C	NCBI36
NG_032953.1:g.5245A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_015631.6:c.1A>G MANE Select	NP_056446.4:p.Met1Val
ENST00000371217.10:c.1A>G MANE Select	ENSP00000360261.5:p.Met1Val
NM_001143973.1:c.1A>G	NP_001137445.1:p.Met1Val
NM_001143973.2:c.1A>G	NP_001137445.1:p.Met1Val
NM_015631.5:c.1A>G	NP_056446.4:p.Met1Val
ENST00000265993.13:c.55A>G	ENSP00000265993.9:p.Met19Val
ENST00000371209.5:c.1A>G	ENSP00000360253.5:p.Met1Val
ENST00000371217.9:c.1A>G	ENSP00000360261.5:p.Met1Val
ENST00000430368.6:c.1A>G	ENSP00000387567.1:p.Met1Val
ENST00000478245.1:n.3A>G
ENST00000497399.1:n.57A>G
ENST00000614499.4:c.1A>G	ENSP00000483364.1:p.Met1Val
ENST00000614499.5:c.55A>G	ENSP00000483364.2:p.Met19Val
ENST00000679485.1:n.25A>G
ENST00000679566.1:c.1A>G	ENSP00000505964.1:p.Met1Val
ENST00000679984.1:c.1A>G	ENSP00000504998.1:p.Met1Val
ENST00000680144.1:c.1A>G	ENSP00000506398.1:p.Met1Val
ENST00000680353.1:c.1A>G	ENSP00000505367.1:p.Met1Val
ENST00000680697.1:n.44A>G
ENST00000680709.1:c.1A>G	ENSP00000505830.1:p.Met1Val
ENST00000681127.1:n.54A>G
ENST00000681739.1:n.56A>G
ENST00000681928.1:c.1A>G	ENSP00000505552.1:p.Met1Val
XM_005269690.1:c.55A>G	XP_005269747.1:p.Met19Val
XM_005269690.2:c.55A>G	XP_005269747.1:p.Met19Val
XM_011539627.1:c.55A>G	XP_011537929.1:p.Met19Val
XM_011539627.2:c.55A>G	XP_011537929.1:p.Met19Val
XM_011539628.1:c.55A>G	XP_011537930.1:p.Met19Val
XM_011539628.2:c.55A>G	XP_011537930.1:p.Met19Val
XM_024447935.1:c.55A>G	XP_024303703.1:p.Met19Val