Canonical Allele Identifier: CA347347757

Gene: DCTN1

Linked Data

• dbSNP Id: rs121909344
• gnomAD v3: 2-74366896-G-C
• gnomAD v4: 2-74366896-G-C
• MyVariant Identifiers: chr2:g.74594023G>C (hg19) ; chr2:g.74366896G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74366896G>C , CM000664.2:g.74366896G>C	GRCh38
NC_000002.11:g.74594023G>C , CM000664.1:g.74594023G>C	GRCh37
NC_000002.10:g.74447531G>C	NCBI36
NG_008735.2:g.30192C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000361874.8:c.2353C>G	ENSP00000354791.4:p.Arg785Gly
ENST00000628224.3:c.2353C>G MANE Select	ENSP00000487279.2:p.Arg785Gly
ENST00000680606.1:c.2302C>G	ENSP00000505612.1:p.Arg768Gly
ENST00000361874.7:c.2353C>G	ENSP00000354791.3:p.Arg785Gly
ENST00000394003.7:c.2332C>G	ENSP00000377571.3:p.Arg778Gly
ENST00000409240.5:c.2242C>G	ENSP00000386406.1:p.Arg748Gly
ENST00000409438.5:c.1951C>G	ENSP00000387270.1:p.Arg651Gly
ENST00000409567.7:c.2293C>G	ENSP00000386843.3:p.Arg765Gly
ENST00000409868.5:c.2302C>G	ENSP00000387327.1:p.Arg768Gly
ENST00000434055.5:c.2242C>G	ENSP00000416711.1:p.Arg748Gly
ENST00000466110.5:n.3170C>G
ENST00000495643.1:n.381C>G
ENST00000497666.1:n.96+2404C>G
ENST00000628224.2:c.2302C>G	ENSP00000487279.1:p.Arg768Gly
ENST00000633691.1:c.1951C>G	ENSP00000487724.1:p.Arg651Gly
NM_001135040.2:c.2293C>G	NP_001128512.1:p.Arg765Gly
NM_001135041.2:c.1951C>G	NP_001128513.1:p.Arg651Gly
NM_001190836.1:c.2242C>G	NP_001177765.1:p.Arg748Gly
NM_001190837.1:c.2332C>G	NP_001177766.1:p.Arg778Gly
NM_004082.4:c.2353C>G	NP_004073.2:p.Arg785Gly
NM_023019.3:c.1951C>G	NP_075408.1:p.Arg651Gly
NR_033935.1:n.2554C>G
NM_001135040.3:c.2293C>G	NP_001128512.1:p.Arg765Gly
NM_001135041.3:c.1951C>G	NP_001128513.1:p.Arg651Gly
NM_001190836.2:c.2242C>G	NP_001177765.1:p.Arg748Gly
NM_001190837.2:c.2332C>G	NP_001177766.1:p.Arg778Gly
NM_001378991.1:c.2302C>G	NP_001365920.1:p.Arg768Gly
NM_001378992.1:c.2284C>G	NP_001365921.1:p.Arg762Gly
NM_004082.5:c.2353C>G MANE Select	NP_004073.2:p.Arg785Gly
NM_023019.4:c.1951C>G	NP_075408.1:p.Arg651Gly
NR_033935.2:n.2333C>G