Canonical Allele Identifier: CA377704396

Gene: TCTN3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95683521C>G , CM000672.2:g.95683521C>G	GRCh38
NC_000010.10:g.97443278C>G , CM000672.1:g.97443278C>G	GRCh37
NC_000010.9:g.97433268C>G	NCBI36
NG_032953.1:g.15623G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_015631.6:c.1203+1G>C MANE Select	NP_056446.4:n.1203+1G>C
ENST00000371217.10:c.1203+1G>C MANE Select	ENSP00000360261.5:n.1203+1G>C
NM_001143973.1:c.759+1G>C	NP_001137445.1:n.759+1G>C
NM_001143973.2:c.759+1G>C	NP_001137445.1:n.759+1G>C
NM_015631.5:c.1203+1G>C	NP_056446.4:n.1203+1G>C
ENST00000265993.13:c.1257+1G>C	ENSP00000265993.9:n.1257+1G>C
ENST00000371209.5:c.1204G>C	ENSP00000360253.5:p.Val402Leu
ENST00000371217.9:c.1203+1G>C	ENSP00000360261.5:n.1203+1G>C
ENST00000430368.6:c.759+1G>C	ENSP00000387567.1:n.759+1G>C
ENST00000614499.4:c.1203+1G>C	ENSP00000483364.1:n.1203+1G>C
ENST00000614499.5:c.1257+1G>C	ENSP00000483364.2:n.1257+1G>C
ENST00000679485.1:n.1227+1G>C
ENST00000679984.1:c.*458+1G>C	ENSP00000504998.1:n.*458+1G>C
ENST00000680144.1:c.1122+1G>C	ENSP00000506398.1:n.1122+1G>C
ENST00000680353.1:c.1203+1G>C	ENSP00000505367.1:n.1203+1G>C
ENST00000680697.1:n.777G>C
ENST00000680709.1:c.966+1G>C	ENSP00000505830.1:n.966+1G>C
ENST00000681739.1:n.1259G>C
ENST00000681928.1:c.*130+3523G>C	ENSP00000505552.1:n.*130+3523G>C
XM_005269690.1:c.1176+1G>C	XP_005269747.1:n.1176+1G>C
XM_005269690.2:c.1176+1G>C	XP_005269747.1:n.1176+1G>C
XM_011539627.1:c.1257+1G>C	XP_011537929.1:n.1257+1G>C
XM_011539627.2:c.1257+1G>C	XP_011537929.1:n.1257+1G>C
XM_011539628.1:c.1257+1G>C	XP_011537930.1:n.1257+1G>C
XM_011539628.2:c.1257+1G>C	XP_011537930.1:n.1257+1G>C
XM_024447935.1:c.1176+1G>C	XP_024303703.1:n.1176+1G>C