Canonical Allele Identifier: CA1722344
Gene: DCTN1 HGNC NCBI
ClinVar Variation:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.74371191C>T , CM000664.2:g.74371191C>T GRCh38
NC_000002.11:g.74598318C>T , CM000664.1:g.74598318C>T GRCh37
NC_000002.10:g.74451826C>T NCBI36
NG_008735.2:g.25897G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361874.8:c.646-15G>A ENSP00000354791.4:n.646-15G>A
ENST00000628224.3:c.646-15G>A MANE Select ENSP00000487279.2:n.646-15G>A
ENST00000680606.1:c.595-15G>A ENSP00000505612.1:n.595-15G>A
ENST00000361874.7:c.646-15G>A ENSP00000354791.3:n.646-15G>A
ENST00000394003.7:c.625-15G>A ENSP00000377571.3:n.625-15G>A
ENST00000409240.5:c.535-15G>A ENSP00000386406.1:n.535-15G>A
ENST00000409438.5:c.244-15G>A ENSP00000387270.1:n.244-15G>A
ENST00000409567.7:c.586-15G>A ENSP00000386843.3:n.586-15G>A
ENST00000409868.5:c.595-15G>A ENSP00000387327.1:n.595-15G>A
ENST00000434055.5:c.535-15G>A ENSP00000416711.1:n.535-15G>A
ENST00000463583.5:n.399-15G>A
ENST00000466110.5:n.852G>A
ENST00000470351.1:n.360-15G>A
ENST00000628224.2:c.595-15G>A ENSP00000487279.1:n.595-15G>A
ENST00000633691.1:c.244-15G>A ENSP00000487724.1:n.244-15G>A
NM_001135040.2:c.586-15G>A NP_001128512.1:n.586-15G>A
NM_001135041.2:c.244-15G>A NP_001128513.1:n.244-15G>A
NM_001190836.1:c.535-15G>A NP_001177765.1:n.535-15G>A
NM_001190837.1:c.625-15G>A NP_001177766.1:n.625-15G>A
NM_004082.4:c.646-15G>A NP_004073.2:n.646-15G>A
NM_023019.3:c.244-15G>A NP_075408.1:n.244-15G>A
NR_033935.1:n.847-15G>A
NM_001135040.3:c.586-15G>A NP_001128512.1:n.586-15G>A
NM_001135041.3:c.244-15G>A NP_001128513.1:n.244-15G>A
NM_001190836.2:c.535-15G>A NP_001177765.1:n.535-15G>A
NM_001190837.2:c.625-15G>A NP_001177766.1:n.625-15G>A
NM_001378991.1:c.595-15G>A NP_001365920.1:n.595-15G>A
NM_001378992.1:c.577-15G>A NP_001365921.1:n.577-15G>A
NM_004082.5:c.646-15G>A MANE Select NP_004073.2:n.646-15G>A
NM_023019.4:c.244-15G>A NP_075408.1:n.244-15G>A
NR_033935.2:n.626-15G>A