Canonical Allele Identifier: CA1721993

Gene: DCTN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74367989G>A , CM000664.2:g.74367989G>A	GRCh38
NC_000002.11:g.74595116G>A , CM000664.1:g.74595116G>A	GRCh37
NC_000002.10:g.74448624G>A	NCBI36
NG_008735.2:g.29099C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004082.5:c.1997C>T MANE Select	NP_004073.2:p.Thr666Met
ENST00000628224.3:c.1997C>T MANE Select	ENSP00000487279.2:p.Thr666Met
NM_001135040.2:c.1937C>T	NP_001128512.1:p.Thr646Met
NM_001135040.3:c.1937C>T	NP_001128512.1:p.Thr646Met
NM_001135041.2:c.1595C>T	NP_001128513.1:p.Thr532Met
NM_001135041.3:c.1595C>T	NP_001128513.1:p.Thr532Met
NM_001190836.1:c.1886C>T	NP_001177765.1:p.Thr629Met
NM_001190836.2:c.1886C>T	NP_001177765.1:p.Thr629Met
NM_001190837.1:c.1976C>T	NP_001177766.1:p.Thr659Met
NM_001190837.2:c.1976C>T	NP_001177766.1:p.Thr659Met
NM_001378991.1:c.1946C>T	NP_001365920.1:p.Thr649Met
NM_001378992.1:c.1928C>T	NP_001365921.1:p.Thr643Met
NM_004082.4:c.1997C>T	NP_004073.2:p.Thr666Met
NM_023019.3:c.1595C>T	NP_075408.1:p.Thr532Met
NM_023019.4:c.1595C>T	NP_075408.1:p.Thr532Met
NR_033935.1:n.2198C>T
NR_033935.2:n.1977C>T
ENST00000361874.7:c.1997C>T	ENSP00000354791.3:p.Thr666Met
ENST00000361874.8:c.1997C>T	ENSP00000354791.4:p.Thr666Met
ENST00000394003.7:c.1976C>T	ENSP00000377571.3:p.Thr659Met
ENST00000409240.5:c.1886C>T	ENSP00000386406.1:p.Thr629Met
ENST00000409438.5:c.1595C>T	ENSP00000387270.1:p.Thr532Met
ENST00000409567.7:c.1937C>T	ENSP00000386843.3:p.Thr646Met
ENST00000409868.5:c.1946C>T	ENSP00000387327.1:p.Thr649Met
ENST00000434055.5:c.1886C>T	ENSP00000416711.1:p.Thr629Met
ENST00000466110.5:n.2814C>T
ENST00000495643.1:n.25C>T
ENST00000497666.1:n.96+1311C>T
ENST00000628224.2:c.1946C>T	ENSP00000487279.1:p.Thr649Met
ENST00000633691.1:c.1595C>T	ENSP00000487724.1:p.Thr532Met
ENST00000680606.1:c.1946C>T	ENSP00000505612.1:p.Thr649Met