Canonical Allele Identifier: CA1722038

Gene: DCTN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74368766C>T , CM000664.2:g.74368766C>T	GRCh38
NC_000002.11:g.74595893C>T , CM000664.1:g.74595893C>T	GRCh37
NC_000002.10:g.74449401C>T	NCBI36
NG_008735.2:g.28322G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004082.5:c.1816G>A MANE Select	NP_004073.2:p.Val606Ile
ENST00000628224.3:c.1816G>A MANE Select	ENSP00000487279.2:p.Val606Ile
NM_001135040.2:c.1756G>A	NP_001128512.1:p.Val586Ile
NM_001135040.3:c.1756G>A	NP_001128512.1:p.Val586Ile
NM_001135041.2:c.1414G>A	NP_001128513.1:p.Val472Ile
NM_001135041.3:c.1414G>A	NP_001128513.1:p.Val472Ile
NM_001190836.1:c.1705G>A	NP_001177765.1:p.Val569Ile
NM_001190836.2:c.1705G>A	NP_001177765.1:p.Val569Ile
NM_001190837.1:c.1795G>A	NP_001177766.1:p.Val599Ile
NM_001190837.2:c.1795G>A	NP_001177766.1:p.Val599Ile
NM_001378991.1:c.1765G>A	NP_001365920.1:p.Val589Ile
NM_001378992.1:c.1747G>A	NP_001365921.1:p.Val583Ile
NM_004082.4:c.1816G>A	NP_004073.2:p.Val606Ile
NM_023019.3:c.1414G>A	NP_075408.1:p.Val472Ile
NM_023019.4:c.1414G>A	NP_075408.1:p.Val472Ile
NR_033935.1:n.2017G>A
NR_033935.2:n.1796G>A
ENST00000361874.7:c.1816G>A	ENSP00000354791.3:p.Val606Ile
ENST00000361874.8:c.1816G>A	ENSP00000354791.4:p.Val606Ile
ENST00000394003.7:c.1795G>A	ENSP00000377571.3:p.Val599Ile
ENST00000409240.5:c.1705G>A	ENSP00000386406.1:p.Val569Ile
ENST00000409438.5:c.1414G>A	ENSP00000387270.1:p.Val472Ile
ENST00000409567.7:c.1756G>A	ENSP00000386843.3:p.Val586Ile
ENST00000409868.5:c.1765G>A	ENSP00000387327.1:p.Val589Ile
ENST00000434055.5:c.1705G>A	ENSP00000416711.1:p.Val569Ile
ENST00000466110.5:n.2037G>A
ENST00000497666.1:n.96+534G>A
ENST00000628224.2:c.1765G>A	ENSP00000487279.1:p.Val589Ile
ENST00000633691.1:c.1414G>A	ENSP00000487724.1:p.Val472Ile
ENST00000680606.1:c.1765G>A	ENSP00000505612.1:p.Val589Ile