Canonical Allele Identifier: CA1721346

Gene: DCTN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74361540G>T , CM000664.2:g.74361540G>T	GRCh38
NC_000002.11:g.74588667G>T , CM000664.1:g.74588667G>T	GRCh37
NC_000002.10:g.74442175G>T	NCBI36
NG_008735.2:g.35548C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004082.5:c.3796C>A MANE Select	NP_004073.2:p.Gln1266Lys
ENST00000628224.3:c.3796C>A MANE Select	ENSP00000487279.2:p.Gln1266Lys
NM_001135040.2:c.3721C>A	NP_001128512.1:p.Gln1241Lys
NM_001135040.3:c.3721C>A	NP_001128512.1:p.Gln1241Lys
NM_001135041.2:c.3379C>A	NP_001128513.1:p.Gln1127Lys
NM_001135041.3:c.3379C>A	NP_001128513.1:p.Gln1127Lys
NM_001190836.1:c.3670C>A	NP_001177765.1:p.Gln1224Lys
NM_001190836.2:c.3670C>A	NP_001177765.1:p.Gln1224Lys
NM_001190837.1:c.3775C>A	NP_001177766.1:p.Gln1259Lys
NM_001190837.2:c.3775C>A	NP_001177766.1:p.Gln1259Lys
NM_001378991.1:c.3745C>A	NP_001365920.1:p.Gln1249Lys
NM_001378992.1:c.3727C>A	NP_001365921.1:p.Gln1243Lys
NM_004082.4:c.3796C>A	NP_004073.2:p.Gln1266Lys
NM_023019.3:c.3394C>A	NP_075408.1:p.Gln1132Lys
NM_023019.4:c.3394C>A	NP_075408.1:p.Gln1132Lys
NR_033935.1:n.4065C>A
NR_033935.2:n.3844C>A
ENST00000361874.7:c.3796C>A	ENSP00000354791.3:p.Gln1266Lys
ENST00000361874.8:c.3781C>A	ENSP00000354791.4:p.Gln1261Lys
ENST00000394003.7:c.3775C>A	ENSP00000377571.3:p.Gln1259Lys
ENST00000409240.5:c.3670C>A	ENSP00000386406.1:p.Gln1224Lys
ENST00000409438.5:c.3379C>A	ENSP00000387270.1:p.Gln1127Lys
ENST00000409567.7:c.3721C>A	ENSP00000386843.3:p.Gln1241Lys
ENST00000409868.5:c.3730C>A	ENSP00000387327.1:p.Gln1244Lys
ENST00000434055.5:c.*1080C>A	ENSP00000416711.1:n.*1080C>A
ENST00000451608.2:c.535C>A	ENSP00000416453.2:p.Gln179Lys
ENST00000466110.5:n.5033C>A
ENST00000491465.5:n.2059C>A
ENST00000497666.1:n.97-3C>A
ENST00000628224.2:c.3730C>A	ENSP00000487279.1:p.Gln1244Lys
ENST00000633691.1:c.3394C>A	ENSP00000487724.1:p.Gln1132Lys
ENST00000680606.1:c.3745C>A	ENSP00000505612.1:p.Gln1249Lys