Canonical Allele Identifier: CA377709075
Gene: TCTN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.95687709G>C , CM000672.2:g.95687709G>C GRCh38
NC_000010.10:g.97447466G>C , CM000672.1:g.97447466G>C GRCh37
NC_000010.9:g.97437456G>C NCBI36
NG_032953.1:g.11435C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371217.10:c.510C>G MANE Select ENSP00000360261.5:p.Asn170Lys
ENST00000614499.5:c.564C>G ENSP00000483364.2:p.Asn188Lys
ENST00000679485.1:n.534C>G
ENST00000679566.1:c.510C>G ENSP00000505964.1:p.Asn170Lys
ENST00000679984.1:c.510C>G ENSP00000504998.1:p.Asn170Lys
ENST00000680144.1:c.510C>G ENSP00000506398.1:p.Asn170Lys
ENST00000680353.1:c.510C>G ENSP00000505367.1:p.Asn170Lys
ENST00000680697.1:n.543-3085C>G
ENST00000680709.1:c.500-550C>G ENSP00000505830.1:n.500-550C>G
ENST00000681127.1:n.563C>G
ENST00000681739.1:n.565C>G
ENST00000681928.1:c.500-354C>G ENSP00000505552.1:n.500-354C>G
ENST00000265993.13:c.564C>G ENSP00000265993.9:p.Asn188Lys
ENST00000371209.5:c.510C>G ENSP00000360253.5:p.Asn170Lys
ENST00000371217.9:c.510C>G ENSP00000360261.5:p.Asn170Lys
ENST00000430368.6:c.500-550C>G ENSP00000387567.1:n.500-550C>G
ENST00000497399.1:n.723-550C>G
ENST00000614499.4:c.510C>G ENSP00000483364.1:p.Asn170Lys
NM_001143973.1:c.500-550C>G NP_001137445.1:n.500-550C>G
NM_015631.5:c.510C>G NP_056446.4:p.Asn170Lys
XM_005269690.1:c.564C>G XP_005269747.1:p.Asn188Lys
XM_011539627.1:c.564C>G XP_011537929.1:p.Asn188Lys
XM_011539628.1:c.564C>G XP_011537930.1:p.Asn188Lys
XM_005269690.2:c.564C>G XP_005269747.1:p.Asn188Lys
XM_011539627.2:c.564C>G XP_011537929.1:p.Asn188Lys
XM_011539628.2:c.564C>G XP_011537930.1:p.Asn188Lys
XM_024447935.1:c.564C>G XP_024303703.1:p.Asn188Lys
NM_015631.6:c.510C>G MANE Select NP_056446.4:p.Asn170Lys
NM_001143973.2:c.500-550C>G NP_001137445.1:n.500-550C>G