Canonical Allele Identifier: CA1721471

Gene: DCTN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74362991T>C , CM000664.2:g.74362991T>C	GRCh38
NC_000002.11:g.74590118T>C , CM000664.1:g.74590118T>C	GRCh37
NC_000002.10:g.74443626T>C	NCBI36
NG_008735.2:g.34097A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004082.5:c.3529+3A>G MANE Select	NP_004073.2:n.3529+3A>G
ENST00000628224.3:c.3529+3A>G MANE Select	ENSP00000487279.2:n.3529+3A>G
NM_001135040.2:c.3454+3A>G	NP_001128512.1:n.3454+3A>G
NM_001135040.3:c.3454+3A>G	NP_001128512.1:n.3454+3A>G
NM_001135041.2:c.3112+3A>G	NP_001128513.1:n.3112+3A>G
NM_001135041.3:c.3112+3A>G	NP_001128513.1:n.3112+3A>G
NM_001190836.1:c.3403+3A>G	NP_001177765.1:n.3403+3A>G
NM_001190836.2:c.3403+3A>G	NP_001177765.1:n.3403+3A>G
NM_001190837.1:c.3508+3A>G	NP_001177766.1:n.3508+3A>G
NM_001190837.2:c.3508+3A>G	NP_001177766.1:n.3508+3A>G
NM_001378991.1:c.3478+3A>G	NP_001365920.1:n.3478+3A>G
NM_001378992.1:c.3460+3A>G	NP_001365921.1:n.3460+3A>G
NM_004082.4:c.3529+3A>G	NP_004073.2:n.3529+3A>G
NM_023019.3:c.3127+3A>G	NP_075408.1:n.3127+3A>G
NM_023019.4:c.3127+3A>G	NP_075408.1:n.3127+3A>G
NR_033935.1:n.3798+3A>G
NR_033935.2:n.3577+3A>G
ENST00000361874.7:c.3529+3A>G	ENSP00000354791.3:n.3529+3A>G
ENST00000361874.8:c.3514+3A>G	ENSP00000354791.4:n.3514+3A>G
ENST00000394003.7:c.3508+3A>G	ENSP00000377571.3:n.3508+3A>G
ENST00000409240.5:c.3403+3A>G	ENSP00000386406.1:n.3403+3A>G
ENST00000409438.5:c.3112+3A>G	ENSP00000387270.1:n.3112+3A>G
ENST00000409567.7:c.3454+3A>G	ENSP00000386843.3:n.3454+3A>G
ENST00000409868.5:c.3463+3A>G	ENSP00000387327.1:n.3463+3A>G
ENST00000434055.5:c.*813+3A>G	ENSP00000416711.1:n.*813+3A>G
ENST00000451608.2:c.268+3A>G	ENSP00000416453.2:n.268+3A>G
ENST00000466110.5:n.4766+3A>G
ENST00000491465.5:n.1792+3A>G
ENST00000497666.1:n.97-1454A>G
ENST00000628224.2:c.3463+3A>G	ENSP00000487279.1:n.3463+3A>G
ENST00000633691.1:c.3127+3A>G	ENSP00000487724.1:n.3127+3A>G
ENST00000680606.1:c.3478+3A>G	ENSP00000505612.1:n.3478+3A>G