Canonical Allele Identifier: CA347370064

Gene: DCTN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74374322C>A , CM000664.2:g.74374322C>A	GRCh38
NC_000002.11:g.74601449C>A , CM000664.1:g.74601449C>A	GRCh37
NC_000002.10:g.74454957C>A	NCBI36
NG_008735.2:g.22766G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004082.5:c.432+1G>T MANE Select	NP_004073.2:n.432+1G>T
ENST00000628224.3:c.432+1G>T MANE Select	ENSP00000487279.2:n.432+1G>T
NM_001135040.2:c.394-2594G>T	NP_001128512.1:n.394-2594G>T
NM_001135040.3:c.394-2594G>T	NP_001128512.1:n.394-2594G>T
NM_001135041.2:c.30+1G>T	NP_001128513.1:n.30+1G>T
NM_001135041.3:c.30+1G>T	NP_001128513.1:n.30+1G>T
NM_001190836.1:c.343-2594G>T	NP_001177765.1:n.343-2594G>T
NM_001190836.2:c.343-2594G>T	NP_001177765.1:n.343-2594G>T
NM_001190837.1:c.411+1G>T	NP_001177766.1:n.411+1G>T
NM_001190837.2:c.411+1G>T	NP_001177766.1:n.411+1G>T
NM_001378991.1:c.381+1G>T	NP_001365920.1:n.381+1G>T
NM_001378992.1:c.364-1374G>T	NP_001365921.1:n.364-1374G>T
NM_004082.4:c.432+1G>T	NP_004073.2:n.432+1G>T
NM_023019.3:c.30+1G>T	NP_075408.1:n.30+1G>T
NM_023019.4:c.30+1G>T	NP_075408.1:n.30+1G>T
NR_033935.1:n.655-2594G>T
NR_033935.2:n.434-2594G>T
ENST00000361874.7:c.432+1G>T	ENSP00000354791.3:n.432+1G>T
ENST00000361874.8:c.432+1G>T	ENSP00000354791.4:n.432+1G>T
ENST00000394003.7:c.411+1G>T	ENSP00000377571.3:n.411+1G>T
ENST00000409240.5:c.343-2594G>T	ENSP00000386406.1:n.343-2594G>T
ENST00000409438.5:c.30+1G>T	ENSP00000387270.1:n.30+1G>T
ENST00000409567.7:c.394-2594G>T	ENSP00000386843.3:n.394-2594G>T
ENST00000409868.5:c.381+1G>T	ENSP00000387327.1:n.381+1G>T
ENST00000434055.5:c.343-2594G>T	ENSP00000416711.1:n.343-2594G>T
ENST00000458655.5:c.453+1G>T	ENSP00000414315.1:n.453+1G>T
ENST00000477966.1:n.373+1G>T
ENST00000628224.2:c.381+1G>T	ENSP00000487279.1:n.381+1G>T
ENST00000633691.1:c.30+1G>T	ENSP00000487724.1:n.30+1G>T
ENST00000680606.1:c.381+1G>T	ENSP00000505612.1:n.381+1G>T