Canonical Allele Identifier: CA1261391847

Gene: DCTN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74363337C= , CM000664.2:g.74363337C=	GRCh38
NC_000002.11:g.74590464C= , CM000664.1:g.74590464C=	GRCh37
NC_000002.10:g.74443972C=	NCBI36
NG_008735.2:g.33751G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361874.8:c.3287G=	ENSP00000354791.4:p.Arg1096=
ENST00000628224.3:c.3302G= MANE Select	ENSP00000487279.2:p.Arg1101=
ENST00000680606.1:c.3251G=	ENSP00000505612.1:p.Arg1084=
ENST00000361874.7:c.3302G=	ENSP00000354791.3:p.Arg1101=
ENST00000394003.7:c.3281G=	ENSP00000377571.3:p.Arg1094=
ENST00000409240.5:c.3176G=	ENSP00000386406.1:p.Arg1059=
ENST00000409438.5:c.2885G=	ENSP00000387270.1:p.Arg962=
ENST00000409567.7:c.3227G=	ENSP00000386843.3:p.Arg1076=
ENST00000409868.5:c.3236G=	ENSP00000387327.1:p.Arg1079=
ENST00000434055.5:c.*586G=	ENSP00000416711.1:n.*586G=
ENST00000451608.2:c.41G=	ENSP00000416453.2:p.Arg14=
ENST00000466110.5:n.4539G=
ENST00000491465.5:n.1565G=
ENST00000497666.1:n.97-1800G=
ENST00000628224.2:c.3236G=	ENSP00000487279.1:p.Arg1079=
ENST00000633691.1:c.2900G=	ENSP00000487724.1:p.Arg967=
NM_001135040.2:c.3227G=	NP_001128512.1:p.Arg1076=
NM_001135041.2:c.2885G=	NP_001128513.1:p.Arg962=
NM_001190836.1:c.3176G=	NP_001177765.1:p.Arg1059=
NM_001190837.1:c.3281G=	NP_001177766.1:p.Arg1094=
NM_004082.4:c.3302G=	NP_004073.2:p.Arg1101=
NM_023019.3:c.2900G=	NP_075408.1:p.Arg967=
NR_033935.1:n.3571G=
NM_001135040.3:c.3227G=	NP_001128512.1:p.Arg1076=
NM_001135041.3:c.2885G=	NP_001128513.1:p.Arg962=
NM_001190836.2:c.3176G=	NP_001177765.1:p.Arg1059=
NM_001190837.2:c.3281G=	NP_001177766.1:p.Arg1094=
NM_001378991.1:c.3251G=	NP_001365920.1:p.Arg1084=
NM_001378992.1:c.3233G=	NP_001365921.1:p.Arg1078=
NM_004082.5:c.3302G= MANE Select	NP_004073.2:p.Arg1101=
NM_023019.4:c.2900G=	NP_075408.1:p.Arg967=
NR_033935.2:n.3350G=