Canonical Allele Identifier: CA1721696

Gene: DCTN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74365896A>C , CM000664.2:g.74365896A>C	GRCh38
NC_000002.11:g.74593023A>C , CM000664.1:g.74593023A>C	GRCh37
NC_000002.10:g.74446531A>C	NCBI36
NG_008735.2:g.31192T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004082.5:c.2883T>G MANE Select	NP_004073.2:p.Ile961Met
ENST00000628224.3:c.2883T>G MANE Select	ENSP00000487279.2:p.Ile961Met
NM_001135040.2:c.2823T>G	NP_001128512.1:p.Ile941Met
NM_001135040.3:c.2823T>G	NP_001128512.1:p.Ile941Met
NM_001135041.2:c.2481T>G	NP_001128513.1:p.Ile827Met
NM_001135041.3:c.2481T>G	NP_001128513.1:p.Ile827Met
NM_001190836.1:c.2772T>G	NP_001177765.1:p.Ile924Met
NM_001190836.2:c.2772T>G	NP_001177765.1:p.Ile924Met
NM_001190837.1:c.2862T>G	NP_001177766.1:p.Ile954Met
NM_001190837.2:c.2862T>G	NP_001177766.1:p.Ile954Met
NM_001378991.1:c.2832T>G	NP_001365920.1:p.Ile944Met
NM_001378992.1:c.2814T>G	NP_001365921.1:p.Ile938Met
NM_004082.4:c.2883T>G	NP_004073.2:p.Ile961Met
NM_023019.3:c.2481T>G	NP_075408.1:p.Ile827Met
NM_023019.4:c.2481T>G	NP_075408.1:p.Ile827Met
NR_033935.1:n.3167T>G
NR_033935.2:n.2946T>G
ENST00000361874.7:c.2883T>G	ENSP00000354791.3:p.Ile961Met
ENST00000361874.8:c.2883T>G	ENSP00000354791.4:p.Ile961Met
ENST00000394003.7:c.2862T>G	ENSP00000377571.3:p.Ile954Met
ENST00000409240.5:c.2772T>G	ENSP00000386406.1:p.Ile924Met
ENST00000409438.5:c.2481T>G	ENSP00000387270.1:p.Ile827Met
ENST00000409567.7:c.2823T>G	ENSP00000386843.3:p.Ile941Met
ENST00000409868.5:c.2832T>G	ENSP00000387327.1:p.Ile944Met
ENST00000434055.5:c.*182T>G	ENSP00000416711.1:n.*182T>G
ENST00000466110.5:n.3862T>G
ENST00000495895.1:n.299T>G
ENST00000497666.1:n.96+3404T>G
ENST00000628224.2:c.2832T>G	ENSP00000487279.1:p.Ile944Met
ENST00000633691.1:c.2481T>G	ENSP00000487724.1:p.Ile827Met
ENST00000680606.1:c.2832T>G	ENSP00000505612.1:p.Ile944Met