Canonical Allele Identifier: CA1722379

Gene: DCTN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74371624C>T , CM000664.2:g.74371624C>T	GRCh38
NC_000002.11:g.74598751C>T , CM000664.1:g.74598751C>T	GRCh37
NC_000002.10:g.74452259C>T	NCBI36
NG_008735.2:g.25464G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361874.8:c.558G>A	ENSP00000354791.4:p.Pro186=
ENST00000628224.3:c.558G>A MANE Select	ENSP00000487279.2:p.Pro186=
ENST00000680606.1:c.507G>A	ENSP00000505612.1:p.Pro169=
ENST00000361874.7:c.558G>A	ENSP00000354791.3:p.Pro186=
ENST00000394003.7:c.537G>A	ENSP00000377571.3:p.Pro179=
ENST00000409240.5:c.447G>A	ENSP00000386406.1:p.Pro149=
ENST00000409438.5:c.156G>A	ENSP00000387270.1:p.Pro52=
ENST00000409567.7:c.498G>A	ENSP00000386843.3:p.Pro166=
ENST00000409868.5:c.507G>A	ENSP00000387327.1:p.Pro169=
ENST00000434055.5:c.447G>A	ENSP00000416711.1:p.Pro149=
ENST00000463583.5:n.311G>A
ENST00000466110.5:n.419G>A
ENST00000470351.1:n.272G>A
ENST00000477966.1:n.499G>A
ENST00000628224.2:c.507G>A	ENSP00000487279.1:p.Pro169=
ENST00000633691.1:c.156G>A	ENSP00000487724.1:p.Pro52=
NM_001135040.2:c.498G>A	NP_001128512.1:p.Pro166=
NM_001135041.2:c.156G>A	NP_001128513.1:p.Pro52=
NM_001190836.1:c.447G>A	NP_001177765.1:p.Pro149=
NM_001190837.1:c.537G>A	NP_001177766.1:p.Pro179=
NM_004082.4:c.558G>A	NP_004073.2:p.Pro186=
NM_023019.3:c.156G>A	NP_075408.1:p.Pro52=
NR_033935.1:n.759G>A
NM_001135040.3:c.498G>A	NP_001128512.1:p.Pro166=
NM_001135041.3:c.156G>A	NP_001128513.1:p.Pro52=
NM_001190836.2:c.447G>A	NP_001177765.1:p.Pro149=
NM_001190837.2:c.537G>A	NP_001177766.1:p.Pro179=
NM_001378991.1:c.507G>A	NP_001365920.1:p.Pro169=
NM_001378992.1:c.489G>A	NP_001365921.1:p.Pro163=
NM_004082.5:c.558G>A MANE Select	NP_004073.2:p.Pro186=
NM_023019.4:c.156G>A	NP_075408.1:p.Pro52=
NR_033935.2:n.538G>A