Canonical Allele Identifier: CA1721492

Gene: DCTN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74363120A>G , CM000664.2:g.74363120A>G	GRCh38
NC_000002.11:g.74590247A>G , CM000664.1:g.74590247A>G	GRCh37
NC_000002.10:g.74443755A>G	NCBI36
NG_008735.2:g.33968T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_004082.5:c.3403T>C MANE Select	NP_004073.2:p.Ser1135Pro
ENST00000628224.3:c.3403T>C MANE Select	ENSP00000487279.2:p.Ser1135Pro
NM_001135040.2:c.3328T>C	NP_001128512.1:p.Ser1110Pro
NM_001135040.3:c.3328T>C	NP_001128512.1:p.Ser1110Pro
NM_001135041.2:c.2986T>C	NP_001128513.1:p.Ser996Pro
NM_001135041.3:c.2986T>C	NP_001128513.1:p.Ser996Pro
NM_001190836.1:c.3277T>C	NP_001177765.1:p.Ser1093Pro
NM_001190836.2:c.3277T>C	NP_001177765.1:p.Ser1093Pro
NM_001190837.1:c.3382T>C	NP_001177766.1:p.Ser1128Pro
NM_001190837.2:c.3382T>C	NP_001177766.1:p.Ser1128Pro
NM_001378991.1:c.3352T>C	NP_001365920.1:p.Ser1118Pro
NM_001378992.1:c.3334T>C	NP_001365921.1:p.Ser1112Pro
NM_004082.4:c.3403T>C	NP_004073.2:p.Ser1135Pro
NM_023019.3:c.3001T>C	NP_075408.1:p.Ser1001Pro
NM_023019.4:c.3001T>C	NP_075408.1:p.Ser1001Pro
NR_033935.1:n.3672T>C
NR_033935.2:n.3451T>C
ENST00000361874.7:c.3403T>C	ENSP00000354791.3:p.Ser1135Pro
ENST00000361874.8:c.3388T>C	ENSP00000354791.4:p.Ser1130Pro
ENST00000394003.7:c.3382T>C	ENSP00000377571.3:p.Ser1128Pro
ENST00000409240.5:c.3277T>C	ENSP00000386406.1:p.Ser1093Pro
ENST00000409438.5:c.2986T>C	ENSP00000387270.1:p.Ser996Pro
ENST00000409567.7:c.3328T>C	ENSP00000386843.3:p.Ser1110Pro
ENST00000409868.5:c.3337T>C	ENSP00000387327.1:p.Ser1113Pro
ENST00000434055.5:c.*687T>C	ENSP00000416711.1:n.*687T>C
ENST00000451608.2:c.142T>C	ENSP00000416453.2:p.Ser48Pro
ENST00000466110.5:n.4640T>C
ENST00000491465.5:n.1666T>C
ENST00000497666.1:n.97-1583T>C
ENST00000628224.2:c.3337T>C	ENSP00000487279.1:p.Ser1113Pro
ENST00000633691.1:c.3001T>C	ENSP00000487724.1:p.Ser1001Pro
ENST00000680606.1:c.3352T>C	ENSP00000505612.1:p.Ser1118Pro