Canonical Allele Identifier: CA1722416

Gene: DCTN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74372935C>T , CM000664.2:g.74372935C>T	GRCh38
NC_000002.11:g.74600062C>T , CM000664.1:g.74600062C>T	GRCh37
NC_000002.10:g.74453570C>T	NCBI36
NG_008735.2:g.24153G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004082.5:c.446G>A MANE Select	NP_004073.2:p.Arg149Gln
ENST00000628224.3:c.446G>A MANE Select	ENSP00000487279.2:p.Arg149Gln
NM_001135040.2:c.394-1207G>A	NP_001128512.1:n.394-1207G>A
NM_001135040.3:c.394-1207G>A	NP_001128512.1:n.394-1207G>A
NM_001135041.2:c.44G>A	NP_001128513.1:p.Arg15Gln
NM_001135041.3:c.44G>A	NP_001128513.1:p.Arg15Gln
NM_001190836.1:c.343-1207G>A	NP_001177765.1:n.343-1207G>A
NM_001190836.2:c.343-1207G>A	NP_001177765.1:n.343-1207G>A
NM_001190837.1:c.425G>A	NP_001177766.1:p.Arg142Gln
NM_001190837.2:c.425G>A	NP_001177766.1:p.Arg142Gln
NM_001378991.1:c.395G>A	NP_001365920.1:p.Arg132Gln
NM_001378992.1:c.377G>A	NP_001365921.1:p.Arg126Gln
NM_004082.4:c.446G>A	NP_004073.2:p.Arg149Gln
NM_023019.3:c.44G>A	NP_075408.1:p.Arg15Gln
NM_023019.4:c.44G>A	NP_075408.1:p.Arg15Gln
NR_033935.1:n.655-1207G>A
NR_033935.2:n.434-1207G>A
ENST00000361874.7:c.446G>A	ENSP00000354791.3:p.Arg149Gln
ENST00000361874.8:c.446G>A	ENSP00000354791.4:p.Arg149Gln
ENST00000394003.7:c.425G>A	ENSP00000377571.3:p.Arg142Gln
ENST00000409240.5:c.343-1207G>A	ENSP00000386406.1:n.343-1207G>A
ENST00000409438.5:c.44G>A	ENSP00000387270.1:p.Arg15Gln
ENST00000409567.7:c.394-1207G>A	ENSP00000386843.3:n.394-1207G>A
ENST00000409868.5:c.395G>A	ENSP00000387327.1:p.Arg132Gln
ENST00000434055.5:c.343-1207G>A	ENSP00000416711.1:n.343-1207G>A
ENST00000458655.5:c.467G>A	ENSP00000414315.1:p.Arg156Gln
ENST00000462813.1:n.281G>A
ENST00000463583.5:n.199G>A
ENST00000477966.1:n.387G>A
ENST00000628224.2:c.395G>A	ENSP00000487279.1:p.Arg132Gln
ENST00000633691.1:c.44G>A	ENSP00000487724.1:p.Arg15Gln
ENST00000680606.1:c.395G>A	ENSP00000505612.1:p.Arg132Gln