Canonical Allele Identifier: CA347343460
Gene: DCTN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 451462
dbSNP Id: rs1437825772
gnomAD v4: 2-74366324-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.74366324T>C , CM000664.2:g.74366324T>C GRCh38
NC_000002.11:g.74593451T>C , CM000664.1:g.74593451T>C GRCh37
NC_000002.10:g.74446959T>C NCBI36
NG_008735.2:g.30764A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361874.8:c.2680A>G ENSP00000354791.4:p.Asn894Asp
ENST00000628224.3:c.2680A>G MANE Select ENSP00000487279.2:p.Asn894Asp
ENST00000680606.1:c.2629A>G ENSP00000505612.1:p.Asn877Asp
ENST00000361874.7:c.2680A>G ENSP00000354791.3:p.Asn894Asp
ENST00000394003.7:c.2659A>G ENSP00000377571.3:p.Asn887Asp
ENST00000409240.5:c.2569A>G ENSP00000386406.1:p.Asn857Asp
ENST00000409438.5:c.2278A>G ENSP00000387270.1:p.Asn760Asp
ENST00000409567.7:c.2620A>G ENSP00000386843.3:p.Asn874Asp
ENST00000409868.5:c.2629A>G ENSP00000387327.1:p.Asn877Asp
ENST00000434055.5:c.2652A>G ENSP00000416711.1:p.Ala884=
ENST00000466110.5:n.3659A>G
ENST00000495643.1:n.546A>G
ENST00000497666.1:n.96+2976A>G
ENST00000628224.2:c.2629A>G ENSP00000487279.1:p.Asn877Asp
ENST00000633691.1:c.2278A>G ENSP00000487724.1:p.Asn760Asp
NM_001135040.2:c.2620A>G NP_001128512.1:p.Asn874Asp
NM_001135041.2:c.2278A>G NP_001128513.1:p.Asn760Asp
NM_001190836.1:c.2569A>G NP_001177765.1:p.Asn857Asp
NM_001190837.1:c.2659A>G NP_001177766.1:p.Asn887Asp
NM_004082.4:c.2680A>G NP_004073.2:p.Asn894Asp
NM_023019.3:c.2278A>G NP_075408.1:p.Asn760Asp
NR_033935.1:n.2964A>G
NM_001135040.3:c.2620A>G NP_001128512.1:p.Asn874Asp
NM_001135041.3:c.2278A>G NP_001128513.1:p.Asn760Asp
NM_001190836.2:c.2569A>G NP_001177765.1:p.Asn857Asp
NM_001190837.2:c.2659A>G NP_001177766.1:p.Asn887Asp
NM_001378991.1:c.2629A>G NP_001365920.1:p.Asn877Asp
NM_001378992.1:c.2611A>G NP_001365921.1:p.Asn871Asp
NM_004082.5:c.2680A>G MANE Select NP_004073.2:p.Asn894Asp
NM_023019.4:c.2278A>G NP_075408.1:p.Asn760Asp
NR_033935.2:n.2743A>G