Canonical Allele Identifier: CA342007
Gene: DCTN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 21390
dbSNP Id: rs67586389

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.74378067C>T , CM000664.2:g.74378067C>T GRCh38
NC_000002.11:g.74605194C>T , CM000664.1:g.74605194C>T GRCh37
NC_000002.10:g.74458702C>T NCBI36
NG_008735.2:g.19021G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000361874.8:c.212G>A ENSP00000354791.4:p.Gly71Glu
ENST00000628224.3:c.212G>A MANE Select ENSP00000487279.2:p.Gly71Glu
ENST00000680606.1:c.161G>A ENSP00000505612.1:p.Gly54Glu
ENST00000361874.7:c.212G>A ENSP00000354791.3:p.Gly71Glu
ENST00000394003.7:c.212G>A ENSP00000377571.3:p.Gly71Glu
ENST00000409240.5:c.161G>A ENSP00000386406.1:p.Gly54Glu
ENST00000409567.7:c.212G>A ENSP00000386843.3:p.Gly71Glu
ENST00000409868.5:c.161G>A ENSP00000387327.1:p.Gly54Glu
ENST00000413111.5:c.161G>A ENSP00000413268.1:p.Gly54Glu
ENST00000417090.1:c.224G>A ENSP00000402509.1:p.Gly75Glu
ENST00000421392.1:c.161G>A ENSP00000409363.1:p.Gly54Glu
ENST00000434055.5:c.161G>A ENSP00000416711.1:p.Gly54Glu
ENST00000437375.1:c.161G>A ENSP00000395312.1:p.Gly54Glu
ENST00000440727.1:c.161G>A ENSP00000400059.1:p.Gly54Glu
ENST00000454119.5:c.161G>A ENSP00000404038.1:p.Gly54Glu
ENST00000458655.5:c.233G>A ENSP00000414315.1:p.Gly78Glu
ENST00000628224.2:c.161G>A ENSP00000487279.1:p.Gly54Glu
NM_001135040.2:c.212G>A NP_001128512.1:p.Gly71Glu
NM_001190836.1:c.161G>A NP_001177765.1:p.Gly54Glu
NM_001190837.1:c.212G>A NP_001177766.1:p.Gly71Glu
NM_004082.4:c.212G>A NP_004073.2:p.Gly71Glu
NR_033935.1:n.473G>A
NM_001135040.3:c.212G>A NP_001128512.1:p.Gly71Glu
NM_001190836.2:c.161G>A NP_001177765.1:p.Gly54Glu
NM_001190837.2:c.212G>A NP_001177766.1:p.Gly71Glu
NM_001378991.1:c.161G>A NP_001365920.1:p.Gly54Glu
NM_001378992.1:c.161G>A NP_001365921.1:p.Gly54Glu
NM_004082.5:c.212G>A MANE Select NP_004073.2:p.Gly71Glu
NR_033935.2:n.252G>A