Canonical Allele Identifier: CA1721472

Gene: DCTN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74363004G>A , CM000664.2:g.74363004G>A	GRCh38
NC_000002.11:g.74590131G>A , CM000664.1:g.74590131G>A	GRCh37
NC_000002.10:g.74443639G>A	NCBI36
NG_008735.2:g.34084C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361874.8:c.3504C>T	ENSP00000354791.4:p.Arg1168=
ENST00000628224.3:c.3519C>T MANE Select	ENSP00000487279.2:p.Arg1173=
ENST00000680606.1:c.3468C>T	ENSP00000505612.1:p.Arg1156=
ENST00000361874.7:c.3519C>T	ENSP00000354791.3:p.Arg1173=
ENST00000394003.7:c.3498C>T	ENSP00000377571.3:p.Arg1166=
ENST00000409240.5:c.3393C>T	ENSP00000386406.1:p.Arg1131=
ENST00000409438.5:c.3102C>T	ENSP00000387270.1:p.Arg1034=
ENST00000409567.7:c.3444C>T	ENSP00000386843.3:p.Arg1148=
ENST00000409868.5:c.3453C>T	ENSP00000387327.1:p.Arg1151=
ENST00000434055.5:c.*803C>T	ENSP00000416711.1:n.*803C>T
ENST00000451608.2:c.258C>T	ENSP00000416453.2:p.Arg86=
ENST00000466110.5:n.4756C>T
ENST00000491465.5:n.1782C>T
ENST00000497666.1:n.97-1467C>T
ENST00000628224.2:c.3453C>T	ENSP00000487279.1:p.Arg1151=
ENST00000633691.1:c.3117C>T	ENSP00000487724.1:p.Arg1039=
NM_001135040.2:c.3444C>T	NP_001128512.1:p.Arg1148=
NM_001135041.2:c.3102C>T	NP_001128513.1:p.Arg1034=
NM_001190836.1:c.3393C>T	NP_001177765.1:p.Arg1131=
NM_001190837.1:c.3498C>T	NP_001177766.1:p.Arg1166=
NM_004082.4:c.3519C>T	NP_004073.2:p.Arg1173=
NM_023019.3:c.3117C>T	NP_075408.1:p.Arg1039=
NR_033935.1:n.3788C>T
NM_001135040.3:c.3444C>T	NP_001128512.1:p.Arg1148=
NM_001135041.3:c.3102C>T	NP_001128513.1:p.Arg1034=
NM_001190836.2:c.3393C>T	NP_001177765.1:p.Arg1131=
NM_001190837.2:c.3498C>T	NP_001177766.1:p.Arg1166=
NM_001378991.1:c.3468C>T	NP_001365920.1:p.Arg1156=
NM_001378992.1:c.3450C>T	NP_001365921.1:p.Arg1150=
NM_004082.5:c.3519C>T MANE Select	NP_004073.2:p.Arg1173=
NM_023019.4:c.3117C>T	NP_075408.1:p.Arg1039=
NR_033935.2:n.3567C>T