Canonical Allele Identifier: CA3098670257

Gene: DCTN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74365702G= , CM000664.2:g.74365702G=	GRCh38
NC_000002.11:g.74592829G= , CM000664.1:g.74592829G=	GRCh37
NC_000002.10:g.74446337G=	NCBI36
NG_008735.2:g.31386C=

Transcript Alleles

HGVS	Amino-acid Change
NM_004082.5:c.2887-45C= MANE Select	NP_004073.2:n.2887-45C=
ENST00000628224.3:c.2887-45C= MANE Select	ENSP00000487279.2:n.2887-45C=
NM_001135040.2:c.2827-45C=	NP_001128512.1:n.2827-45C=
NM_001135040.3:c.2827-45C=	NP_001128512.1:n.2827-45C=
NM_001135041.2:c.2485-45C=	NP_001128513.1:n.2485-45C=
NM_001135041.3:c.2485-45C=	NP_001128513.1:n.2485-45C=
NM_001190836.1:c.2776-45C=	NP_001177765.1:n.2776-45C=
NM_001190836.2:c.2776-45C=	NP_001177765.1:n.2776-45C=
NM_001190837.1:c.2866-45C=	NP_001177766.1:n.2866-45C=
NM_001190837.2:c.2866-45C=	NP_001177766.1:n.2866-45C=
NM_001378991.1:c.2836-45C=	NP_001365920.1:n.2836-45C=
NM_001378992.1:c.2818-45C=	NP_001365921.1:n.2818-45C=
NM_004082.4:c.2887-45C=	NP_004073.2:n.2887-45C=
NM_023019.3:c.2485-45C=	NP_075408.1:n.2485-45C=
NM_023019.4:c.2485-45C=	NP_075408.1:n.2485-45C=
NR_033935.1:n.3171-45C=
NR_033935.2:n.2950-45C=
ENST00000361874.7:c.2887-45C=	ENSP00000354791.3:n.2887-45C=
ENST00000361874.8:c.2887-45C=	ENSP00000354791.4:n.2887-45C=
ENST00000394003.7:c.2866-45C=	ENSP00000377571.3:n.2866-45C=
ENST00000409240.5:c.2776-45C=	ENSP00000386406.1:n.2776-45C=
ENST00000409438.5:c.2485-45C=	ENSP00000387270.1:n.2485-45C=
ENST00000409567.7:c.2827-45C=	ENSP00000386843.3:n.2827-45C=
ENST00000409868.5:c.2836-45C=	ENSP00000387327.1:n.2836-45C=
ENST00000434055.5:c.*186-45C=	ENSP00000416711.1:n.*186-45C=
ENST00000466110.5:n.3866-45C=
ENST00000495895.1:n.303-45C=
ENST00000497666.1:n.96+3598C=
ENST00000628224.2:c.2836-45C=	ENSP00000487279.1:n.2836-45C=
ENST00000633691.1:c.2485-45C=	ENSP00000487724.1:n.2485-45C=
ENST00000680606.1:c.2836-45C=	ENSP00000505612.1:n.2836-45C=