Canonical Allele Identifier: CA5620935

Gene: TCTN3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95683562C>G , CM000672.2:g.95683562C>G	GRCh38
NC_000010.10:g.97443319C>G , CM000672.1:g.97443319C>G	GRCh37
NC_000010.9:g.97433309C>G	NCBI36
NG_032953.1:g.15582G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371217.10:c.1163G>C MANE Select	ENSP00000360261.5:p.Gly388Ala
ENST00000614499.5:c.1217G>C	ENSP00000483364.2:p.Gly406Ala
ENST00000679485.1:n.1187G>C
ENST00000679984.1:c.*418G>C	ENSP00000504998.1:n.*418G>C
ENST00000680144.1:c.1082G>C	ENSP00000506398.1:p.Gly361Ala
ENST00000680353.1:c.1163G>C	ENSP00000505367.1:p.Gly388Ala
ENST00000680697.1:n.736G>C
ENST00000680709.1:c.926G>C	ENSP00000505830.1:p.Gly309Ala
ENST00000681739.1:n.1218G>C
ENST00000681928.1:c.*130+3482G>C	ENSP00000505552.1:n.*130+3482G>C
ENST00000265993.13:c.1217G>C	ENSP00000265993.9:p.Gly406Ala
ENST00000371209.5:c.1163G>C	ENSP00000360253.5:p.Gly388Ala
ENST00000371217.9:c.1163G>C	ENSP00000360261.5:p.Gly388Ala
ENST00000430368.6:c.719G>C	ENSP00000387567.1:p.Gly240Ala
ENST00000614499.4:c.1163G>C	ENSP00000483364.1:p.Gly388Ala
NM_001143973.1:c.719G>C	NP_001137445.1:p.Gly240Ala
NM_015631.5:c.1163G>C	NP_056446.4:p.Gly388Ala
XM_005269690.1:c.1136G>C	XP_005269747.1:p.Gly379Ala
XM_011539627.1:c.1217G>C	XP_011537929.1:p.Gly406Ala
XM_011539628.1:c.1217G>C	XP_011537930.1:p.Gly406Ala
XM_005269690.2:c.1136G>C	XP_005269747.1:p.Gly379Ala
XM_011539627.2:c.1217G>C	XP_011537929.1:p.Gly406Ala
XM_011539628.2:c.1217G>C	XP_011537930.1:p.Gly406Ala
XM_024447935.1:c.1136G>C	XP_024303703.1:p.Gly379Ala
NM_015631.6:c.1163G>C MANE Select	NP_056446.4:p.Gly388Ala
NM_001143973.2:c.719G>C	NP_001137445.1:p.Gly240Ala