Canonical Allele Identifier: CA377704485

Gene: TCTN3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95683565A>C , CM000672.2:g.95683565A>C	GRCh38
NC_000010.10:g.97443322A>C , CM000672.1:g.97443322A>C	GRCh37
NC_000010.9:g.97433312A>C	NCBI36
NG_032953.1:g.15579T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371217.10:c.1160T>G MANE Select	ENSP00000360261.5:p.Val387Gly
ENST00000614499.5:c.1214T>G	ENSP00000483364.2:p.Val405Gly
ENST00000679485.1:n.1184T>G
ENST00000679984.1:c.*415T>G	ENSP00000504998.1:n.*415T>G
ENST00000680144.1:c.1079T>G	ENSP00000506398.1:p.Val360Gly
ENST00000680353.1:c.1160T>G	ENSP00000505367.1:p.Val387Gly
ENST00000680697.1:n.733T>G
ENST00000680709.1:c.923T>G	ENSP00000505830.1:p.Val308Gly
ENST00000681739.1:n.1215T>G
ENST00000681928.1:c.*130+3479T>G	ENSP00000505552.1:n.*130+3479T>G
ENST00000265993.13:c.1214T>G	ENSP00000265993.9:p.Val405Gly
ENST00000371209.5:c.1160T>G	ENSP00000360253.5:p.Val387Gly
ENST00000371217.9:c.1160T>G	ENSP00000360261.5:p.Val387Gly
ENST00000430368.6:c.716T>G	ENSP00000387567.1:p.Val239Gly
ENST00000614499.4:c.1160T>G	ENSP00000483364.1:p.Val387Gly
NM_001143973.1:c.716T>G	NP_001137445.1:p.Val239Gly
NM_015631.5:c.1160T>G	NP_056446.4:p.Val387Gly
XM_005269690.1:c.1133T>G	XP_005269747.1:p.Val378Gly
XM_011539627.1:c.1214T>G	XP_011537929.1:p.Val405Gly
XM_011539628.1:c.1214T>G	XP_011537930.1:p.Val405Gly
XM_005269690.2:c.1133T>G	XP_005269747.1:p.Val378Gly
XM_011539627.2:c.1214T>G	XP_011537929.1:p.Val405Gly
XM_011539628.2:c.1214T>G	XP_011537930.1:p.Val405Gly
XM_024447935.1:c.1133T>G	XP_024303703.1:p.Val378Gly
NM_015631.6:c.1160T>G MANE Select	NP_056446.4:p.Val387Gly
NM_001143973.2:c.716T>G	NP_001137445.1:p.Val239Gly