Canonical Allele Identifier: CA1722212

Gene: DCTN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74370247C>T , CM000664.2:g.74370247C>T	GRCh38
NC_000002.11:g.74597374C>T , CM000664.1:g.74597374C>T	GRCh37
NC_000002.10:g.74450882C>T	NCBI36
NG_008735.2:g.26841G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004082.5:c.1226G>A MANE Select	NP_004073.2:p.Arg409Gln
ENST00000628224.3:c.1226G>A MANE Select	ENSP00000487279.2:p.Arg409Gln
NM_001135040.2:c.1166G>A	NP_001128512.1:p.Arg389Gln
NM_001135040.3:c.1166G>A	NP_001128512.1:p.Arg389Gln
NM_001135041.2:c.824G>A	NP_001128513.1:p.Arg275Gln
NM_001135041.3:c.824G>A	NP_001128513.1:p.Arg275Gln
NM_001190836.1:c.1115G>A	NP_001177765.1:p.Arg372Gln
NM_001190836.2:c.1115G>A	NP_001177765.1:p.Arg372Gln
NM_001190837.1:c.1205G>A	NP_001177766.1:p.Arg402Gln
NM_001190837.2:c.1205G>A	NP_001177766.1:p.Arg402Gln
NM_001378991.1:c.1175G>A	NP_001365920.1:p.Arg392Gln
NM_001378992.1:c.1157G>A	NP_001365921.1:p.Arg386Gln
NM_004082.4:c.1226G>A	NP_004073.2:p.Arg409Gln
NM_023019.3:c.824G>A	NP_075408.1:p.Arg275Gln
NM_023019.4:c.824G>A	NP_075408.1:p.Arg275Gln
NR_033935.1:n.1427G>A
NR_033935.2:n.1206G>A
ENST00000361874.7:c.1226G>A	ENSP00000354791.3:p.Arg409Gln
ENST00000361874.8:c.1226G>A	ENSP00000354791.4:p.Arg409Gln
ENST00000394003.7:c.1205G>A	ENSP00000377571.3:p.Arg402Gln
ENST00000409240.5:c.1115G>A	ENSP00000386406.1:p.Arg372Gln
ENST00000409438.5:c.824G>A	ENSP00000387270.1:p.Arg275Gln
ENST00000409567.7:c.1166G>A	ENSP00000386843.3:p.Arg389Gln
ENST00000409868.5:c.1175G>A	ENSP00000387327.1:p.Arg392Gln
ENST00000434055.5:c.1115G>A	ENSP00000416711.1:p.Arg372Gln
ENST00000466110.5:n.1447G>A
ENST00000628224.2:c.1175G>A	ENSP00000487279.1:p.Arg392Gln
ENST00000633691.1:c.824G>A	ENSP00000487724.1:p.Arg275Gln
ENST00000680606.1:c.1175G>A	ENSP00000505612.1:p.Arg392Gln