Canonical Allele Identifier: CA1721809

Gene: DCTN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74366536G>C , CM000664.2:g.74366536G>C	GRCh38
NC_000002.11:g.74593663G>C , CM000664.1:g.74593663G>C	GRCh37
NC_000002.10:g.74447171G>C	NCBI36
NG_008735.2:g.30552C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004082.5:c.2551C>G MANE Select	NP_004073.2:p.Leu851Val
ENST00000628224.3:c.2551C>G MANE Select	ENSP00000487279.2:p.Leu851Val
NM_001135040.2:c.2491C>G	NP_001128512.1:p.Leu831Val
NM_001135040.3:c.2491C>G	NP_001128512.1:p.Leu831Val
NM_001135041.2:c.2149C>G	NP_001128513.1:p.Leu717Val
NM_001135041.3:c.2149C>G	NP_001128513.1:p.Leu717Val
NM_001190836.1:c.2440C>G	NP_001177765.1:p.Leu814Val
NM_001190836.2:c.2440C>G	NP_001177765.1:p.Leu814Val
NM_001190837.1:c.2530C>G	NP_001177766.1:p.Leu844Val
NM_001190837.2:c.2530C>G	NP_001177766.1:p.Leu844Val
NM_001378991.1:c.2500C>G	NP_001365920.1:p.Leu834Val
NM_001378992.1:c.2482C>G	NP_001365921.1:p.Leu828Val
NM_004082.4:c.2551C>G	NP_004073.2:p.Leu851Val
NM_023019.3:c.2149C>G	NP_075408.1:p.Leu717Val
NM_023019.4:c.2149C>G	NP_075408.1:p.Leu717Val
NR_033935.1:n.2752C>G
NR_033935.2:n.2531C>G
ENST00000361874.7:c.2551C>G	ENSP00000354791.3:p.Leu851Val
ENST00000361874.8:c.2551C>G	ENSP00000354791.4:p.Leu851Val
ENST00000394003.7:c.2530C>G	ENSP00000377571.3:p.Leu844Val
ENST00000409240.5:c.2440C>G	ENSP00000386406.1:p.Leu814Val
ENST00000409438.5:c.2149C>G	ENSP00000387270.1:p.Leu717Val
ENST00000409567.7:c.2491C>G	ENSP00000386843.3:p.Leu831Val
ENST00000409868.5:c.2500C>G	ENSP00000387327.1:p.Leu834Val
ENST00000434055.5:c.2440C>G	ENSP00000416711.1:p.Leu814Val
ENST00000466110.5:n.3530C>G
ENST00000495643.1:n.495-161C>G
ENST00000497666.1:n.96+2764C>G
ENST00000628224.2:c.2500C>G	ENSP00000487279.1:p.Leu834Val
ENST00000633691.1:c.2149C>G	ENSP00000487724.1:p.Leu717Val
ENST00000680606.1:c.2500C>G	ENSP00000505612.1:p.Leu834Val