Canonical Allele Identifier: CA1721712
Community Standard Title: NM_004082.5(DCTN1):c.2794C>T (p.Arg932Cys)
Gene: DCTN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.74365985G>A , CM000664.2:g.74365985G>A GRCh38
NC_000002.11:g.74593112G>A , CM000664.1:g.74593112G>A GRCh37
NC_000002.10:g.74446620G>A NCBI36
NG_008735.2:g.31103C>T

Transcript Alleles

HGVS Amino-acid Change
NM_004082.5:c.2794C>T MANE Select NP_004073.2:p.Arg932Cys
ENST00000628224.3:c.2794C>T MANE Select ENSP00000487279.2:p.Arg932Cys
NM_001135040.2:c.2734C>T NP_001128512.1:p.Arg912Cys
NM_001135040.3:c.2734C>T NP_001128512.1:p.Arg912Cys
NM_001135041.2:c.2392C>T NP_001128513.1:p.Arg798Cys
NM_001135041.3:c.2392C>T NP_001128513.1:p.Arg798Cys
NM_001190836.1:c.2683C>T NP_001177765.1:p.Arg895Cys
NM_001190836.2:c.2683C>T NP_001177765.1:p.Arg895Cys
NM_001190837.1:c.2773C>T NP_001177766.1:p.Arg925Cys
NM_001190837.2:c.2773C>T NP_001177766.1:p.Arg925Cys
NM_001378991.1:c.2743C>T NP_001365920.1:p.Arg915Cys
NM_001378992.1:c.2725C>T NP_001365921.1:p.Arg909Cys
NM_004082.4:c.2794C>T NP_004073.2:p.Arg932Cys
NM_023019.3:c.2392C>T NP_075408.1:p.Arg798Cys
NM_023019.4:c.2392C>T NP_075408.1:p.Arg798Cys
NR_033935.1:n.3078C>T
NR_033935.2:n.2857C>T
ENST00000361874.7:c.2794C>T ENSP00000354791.3:p.Arg932Cys
ENST00000361874.8:c.2794C>T ENSP00000354791.4:p.Arg932Cys
ENST00000394003.7:c.2773C>T ENSP00000377571.3:p.Arg925Cys
ENST00000409240.5:c.2683C>T ENSP00000386406.1:p.Arg895Cys
ENST00000409438.5:c.2392C>T ENSP00000387270.1:p.Arg798Cys
ENST00000409567.7:c.2734C>T ENSP00000386843.3:p.Arg912Cys
ENST00000409868.5:c.2743C>T ENSP00000387327.1:p.Arg915Cys
ENST00000434055.5:c.*93C>T ENSP00000416711.1:n.*93C>T
ENST00000466110.5:n.3773C>T
ENST00000495643.1:n.660C>T
ENST00000495895.1:n.210C>T
ENST00000497666.1:n.96+3315C>T
ENST00000628224.2:c.2743C>T ENSP00000487279.1:p.Arg915Cys
ENST00000633691.1:c.2392C>T ENSP00000487724.1:p.Arg798Cys
ENST00000680606.1:c.2743C>T ENSP00000505612.1:p.Arg915Cys