Canonical Allele Identifier: CA211792991

Gene: TCTN3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95664203T>G , CM000672.2:g.95664203T>G	GRCh38
NC_000010.10:g.97423960T>G , CM000672.1:g.97423960T>G	GRCh37
NC_000010.9:g.97413950T>G	NCBI36
NG_032953.1:g.34941A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371217.10:c.1688A>C MANE Select	ENSP00000360261.5:p.Asp563Ala
ENST00000614499.5:c.1727A>C	ENSP00000483364.2:p.Asp576Ala
ENST00000679984.1:c.*928A>C	ENSP00000504998.1:n.*928A>C
ENST00000680144.1:c.1592A>C	ENSP00000506398.1:p.Asp531Ala
ENST00000680353.1:c.1439A>C	ENSP00000505367.1:p.Asp480Ala
ENST00000680697.1:n.1883A>C
ENST00000680709.1:c.1436A>C	ENSP00000505830.1:p.Asp479Ala
ENST00000680781.1:c.345A>C
ENST00000681185.1:n.390A>C
ENST00000681739.1:n.2069A>C
ENST00000681928.1:c.*228A>C	ENSP00000505552.1:n.*228A>C
ENST00000265993.13:c.1742A>C	ENSP00000265993.9:p.Asp581Ala
ENST00000371217.9:c.1688A>C	ENSP00000360261.5:p.Asp563Ala
ENST00000430368.6:c.1244A>C	ENSP00000387567.1:p.Asp415Ala
ENST00000614499.4:c.1688A>C	ENSP00000483364.1:p.Asp563Ala
NM_001143973.1:c.1244A>C	NP_001137445.1:p.Asp415Ala
NM_015631.5:c.1688A>C	NP_056446.4:p.Asp563Ala
XM_005269690.1:c.1661A>C	XP_005269747.1:p.Asp554Ala
XM_011539627.1:c.1727A>C	XP_011537929.1:p.Asp576Ala
XM_011539628.1:c.1604A>C	XP_011537930.1:p.Asp535Ala
XM_005269690.2:c.1661A>C	XP_005269747.1:p.Asp554Ala
XM_011539627.2:c.1727A>C	XP_011537929.1:p.Asp576Ala
XM_011539628.2:c.1604A>C	XP_011537930.1:p.Asp535Ala
XM_024447935.1:c.1646A>C	XP_024303703.1:p.Asp549Ala
NM_015631.6:c.1688A>C MANE Select	NP_056446.4:p.Asp563Ala
NM_001143973.2:c.1244A>C	NP_001137445.1:p.Asp415Ala