Canonical Allele Identifier: CA427030143

Gene: DCTN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74366325G>A , CM000664.2:g.74366325G>A	GRCh38
NC_000002.11:g.74593452G>A , CM000664.1:g.74593452G>A	GRCh37
NC_000002.10:g.74446960G>A	NCBI36
NG_008735.2:g.30763C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361874.8:c.2679C>T	ENSP00000354791.4:p.Cys893=
ENST00000628224.3:c.2679C>T MANE Select	ENSP00000487279.2:p.Cys893=
ENST00000680606.1:c.2628C>T	ENSP00000505612.1:p.Cys876=
ENST00000361874.7:c.2679C>T	ENSP00000354791.3:p.Cys893=
ENST00000394003.7:c.2658C>T	ENSP00000377571.3:p.Cys886=
ENST00000409240.5:c.2568C>T	ENSP00000386406.1:p.Cys856=
ENST00000409438.5:c.2277C>T	ENSP00000387270.1:p.Cys759=
ENST00000409567.7:c.2619C>T	ENSP00000386843.3:p.Cys873=
ENST00000409868.5:c.2628C>T	ENSP00000387327.1:p.Cys876=
ENST00000434055.5:c.2651C>T	ENSP00000416711.1:p.Ala884Val
ENST00000466110.5:n.3658C>T
ENST00000495643.1:n.545C>T
ENST00000497666.1:n.96+2975C>T
ENST00000628224.2:c.2628C>T	ENSP00000487279.1:p.Cys876=
ENST00000633691.1:c.2277C>T	ENSP00000487724.1:p.Cys759=
NM_001135040.2:c.2619C>T	NP_001128512.1:p.Cys873=
NM_001135041.2:c.2277C>T	NP_001128513.1:p.Cys759=
NM_001190836.1:c.2568C>T	NP_001177765.1:p.Cys856=
NM_001190837.1:c.2658C>T	NP_001177766.1:p.Cys886=
NM_004082.4:c.2679C>T	NP_004073.2:p.Cys893=
NM_023019.3:c.2277C>T	NP_075408.1:p.Cys759=
NR_033935.1:n.2963C>T
NM_001135040.3:c.2619C>T	NP_001128512.1:p.Cys873=
NM_001135041.3:c.2277C>T	NP_001128513.1:p.Cys759=
NM_001190836.2:c.2568C>T	NP_001177765.1:p.Cys856=
NM_001190837.2:c.2658C>T	NP_001177766.1:p.Cys886=
NM_001378991.1:c.2628C>T	NP_001365920.1:p.Cys876=
NM_001378992.1:c.2610C>T	NP_001365921.1:p.Cys870=
NM_004082.5:c.2679C>T MANE Select	NP_004073.2:p.Cys893=
NM_023019.4:c.2277C>T	NP_075408.1:p.Cys759=
NR_033935.2:n.2742C>T