Canonical Allele Identifier: CA1261390959

Gene: DCTN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74361590G= , CM000664.2:g.74361590G=	GRCh38
NC_000002.11:g.74588717G= , CM000664.1:g.74588717G=	GRCh37
NC_000002.10:g.74442225G=	NCBI36
NG_008735.2:g.35498C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361874.8:c.3731C=	ENSP00000354791.4:p.Thr1244=
ENST00000628224.3:c.3746C= MANE Select	ENSP00000487279.2:p.Thr1249=
ENST00000680606.1:c.3695C=	ENSP00000505612.1:p.Thr1232=
ENST00000361874.7:c.3746C=	ENSP00000354791.3:p.Thr1249=
ENST00000394003.7:c.3725C=	ENSP00000377571.3:p.Thr1242=
ENST00000409240.5:c.3620C=	ENSP00000386406.1:p.Thr1207=
ENST00000409438.5:c.3329C=	ENSP00000387270.1:p.Thr1110=
ENST00000409567.7:c.3671C=	ENSP00000386843.3:p.Thr1224=
ENST00000409868.5:c.3680C=	ENSP00000387327.1:p.Thr1227=
ENST00000434055.5:c.*1030C=	ENSP00000416711.1:n.*1030C=
ENST00000451608.2:c.485C=	ENSP00000416453.2:p.Thr162=
ENST00000466110.5:n.4983C=
ENST00000491465.5:n.2009C=
ENST00000497666.1:n.97-53C=
ENST00000628224.2:c.3680C=	ENSP00000487279.1:p.Thr1227=
ENST00000633691.1:c.3344C=	ENSP00000487724.1:p.Thr1115=
NM_001135040.2:c.3671C=	NP_001128512.1:p.Thr1224=
NM_001135041.2:c.3329C=	NP_001128513.1:p.Thr1110=
NM_001190836.1:c.3620C=	NP_001177765.1:p.Thr1207=
NM_001190837.1:c.3725C=	NP_001177766.1:p.Thr1242=
NM_004082.4:c.3746C=	NP_004073.2:p.Thr1249=
NM_023019.3:c.3344C=	NP_075408.1:p.Thr1115=
NR_033935.1:n.4015C=
NM_001135040.3:c.3671C=	NP_001128512.1:p.Thr1224=
NM_001135041.3:c.3329C=	NP_001128513.1:p.Thr1110=
NM_001190836.2:c.3620C=	NP_001177765.1:p.Thr1207=
NM_001190837.2:c.3725C=	NP_001177766.1:p.Thr1242=
NM_001378991.1:c.3695C=	NP_001365920.1:p.Thr1232=
NM_001378992.1:c.3677C=	NP_001365921.1:p.Thr1226=
NM_004082.5:c.3746C= MANE Select	NP_004073.2:p.Thr1249=
NM_023019.4:c.3344C=	NP_075408.1:p.Thr1115=
NR_033935.2:n.3794C=