Canonical Allele Identifier: CA5620765

Gene: TCTN3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95664295A>G , CM000672.2:g.95664295A>G	GRCh38
NC_000010.10:g.97424052A>G , CM000672.1:g.97424052A>G	GRCh37
NC_000010.9:g.97414042A>G	NCBI36
NG_032953.1:g.34849T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371217.10:c.1596T>C MANE Select	ENSP00000360261.5:p.Ser532=
ENST00000614499.5:c.1635T>C	ENSP00000483364.2:p.Ser545=
ENST00000679984.1:c.*836T>C	ENSP00000504998.1:n.*836T>C
ENST00000680144.1:c.1500T>C	ENSP00000506398.1:p.Ser500=
ENST00000680353.1:c.1347T>C	ENSP00000505367.1:p.Ser449=
ENST00000680697.1:n.1791T>C
ENST00000680709.1:c.1344T>C	ENSP00000505830.1:p.Ser448=
ENST00000680781.1:c.253T>C
ENST00000681185.1:n.298T>C
ENST00000681739.1:n.1977T>C
ENST00000681928.1:c.*136T>C	ENSP00000505552.1:n.*136T>C
ENST00000265993.13:c.1650T>C	ENSP00000265993.9:p.Ser550=
ENST00000371217.9:c.1596T>C	ENSP00000360261.5:p.Ser532=
ENST00000430368.6:c.1152T>C	ENSP00000387567.1:p.Ser384=
ENST00000614499.4:c.1596T>C	ENSP00000483364.1:p.Ser532=
NM_001143973.1:c.1152T>C	NP_001137445.1:p.Ser384=
NM_015631.5:c.1596T>C	NP_056446.4:p.Ser532=
XM_005269690.1:c.1569T>C	XP_005269747.1:p.Ser523=
XM_011539627.1:c.1635T>C	XP_011537929.1:p.Ser545=
XM_011539628.1:c.1512T>C	XP_011537930.1:p.Ser504=
XM_005269690.2:c.1569T>C	XP_005269747.1:p.Ser523=
XM_011539627.2:c.1635T>C	XP_011537929.1:p.Ser545=
XM_011539628.2:c.1512T>C	XP_011537930.1:p.Ser504=
XM_024447935.1:c.1554T>C	XP_024303703.1:p.Ser518=
NM_015631.6:c.1596T>C MANE Select	NP_056446.4:p.Ser532=
NM_001143973.2:c.1152T>C	NP_001137445.1:p.Ser384=