Canonical Allele Identifier: CA1721332

Gene: DCTN1

Linked Data

• ClinVar Variation Id: 337066
• ClinVar RCV Id: RCV000303678 ; RCV000407896
• dbSNP Id: rs11555696
• ExAC: 2:74588605 G / A
• gnomAD v2: 2-74588605-G-A
• gnomAD v3: 2-74361478-G-A
• gnomAD v4: 2-74361478-G-A
• MyVariant Identifiers: chr2:g.74588605G>A (hg19) ; chr2:g.74361478G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74361478G>A , CM000664.2:g.74361478G>A	GRCh38
NC_000002.11:g.74588605G>A , CM000664.1:g.74588605G>A	GRCh37
NC_000002.10:g.74442113G>A	NCBI36
NG_008735.2:g.35610C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361874.8:c.*21C>T	ENSP00000354791.4:n.*21C>T
ENST00000628224.3:c.*21C>T MANE Select	ENSP00000487279.2:n.*21C>T
ENST00000680606.1:c.*21C>T	ENSP00000505612.1:n.*21C>T
ENST00000361874.7:c.*21C>T	ENSP00000354791.3:n.*21C>T
ENST00000394003.7:c.*21C>T	ENSP00000377571.3:n.*21C>T
ENST00000409240.5:c.*21C>T	ENSP00000386406.1:n.*21C>T
ENST00000409438.5:c.*21C>T	ENSP00000387270.1:n.*21C>T
ENST00000409868.5:c.*21C>T	ENSP00000387327.1:n.*21C>T
ENST00000434055.5:c.*1142C>T	ENSP00000416711.1:n.*1142C>T
ENST00000451608.2:c.597C>T	ENSP00000416453.2:n.597C>T
ENST00000466110.5:n.5095C>T
ENST00000491465.5:n.2121C>T
ENST00000497666.1:n.156C>T
ENST00000628224.2:c.*21C>T	ENSP00000487279.1:n.*21C>T
ENST00000633691.1:c.*21C>T	ENSP00000487724.1:n.*21C>T
NM_001135040.2:c.*21C>T	NP_001128512.1:n.*21C>T
NM_001135041.2:c.*21C>T	NP_001128513.1:n.*21C>T
NM_001190836.1:c.*21C>T	NP_001177765.1:n.*21C>T
NM_001190837.1:c.*21C>T	NP_001177766.1:n.*21C>T
NM_004082.4:c.*21C>T	NP_004073.2:n.*21C>T
NM_023019.3:c.*21C>T	NP_075408.1:n.*21C>T
NR_033935.1:n.4127C>T
NM_001135040.3:c.*21C>T	NP_001128512.1:n.*21C>T
NM_001135041.3:c.*21C>T	NP_001128513.1:n.*21C>T
NM_001190836.2:c.*21C>T	NP_001177765.1:n.*21C>T
NM_001190837.2:c.*21C>T	NP_001177766.1:n.*21C>T
NM_001378991.1:c.*21C>T	NP_001365920.1:n.*21C>T
NM_001378992.1:c.*21C>T	NP_001365921.1:n.*21C>T
NM_004082.5:c.*21C>T MANE Select	NP_004073.2:n.*21C>T
NM_023019.4:c.*21C>T	NP_075408.1:n.*21C>T
NR_033935.2:n.3906C>T