Canonical Allele Identifier: CA1721441

Gene: DCTN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74362702A>G , CM000664.2:g.74362702A>G	GRCh38
NC_000002.11:g.74589829A>G , CM000664.1:g.74589829A>G	GRCh37
NC_000002.10:g.74443337A>G	NCBI36
NG_008735.2:g.34386T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361874.8:c.3542T>C	ENSP00000354791.4:p.Met1181Thr
ENST00000628224.3:c.3557T>C MANE Select	ENSP00000487279.2:p.Met1186Thr
ENST00000680606.1:c.3506T>C	ENSP00000505612.1:p.Met1169Thr
ENST00000361874.7:c.3557T>C	ENSP00000354791.3:p.Met1186Thr
ENST00000394003.7:c.3536T>C	ENSP00000377571.3:p.Met1179Thr
ENST00000409240.5:c.3431T>C	ENSP00000386406.1:p.Met1144Thr
ENST00000409438.5:c.3140T>C	ENSP00000387270.1:p.Met1047Thr
ENST00000409567.7:c.3482T>C	ENSP00000386843.3:p.Met1161Thr
ENST00000409868.5:c.3491T>C	ENSP00000387327.1:p.Met1164Thr
ENST00000434055.5:c.*841T>C	ENSP00000416711.1:n.*841T>C
ENST00000451608.2:c.296T>C	ENSP00000416453.2:p.Met99Thr
ENST00000466110.5:n.4794T>C
ENST00000491465.5:n.1820T>C
ENST00000492717.1:n.228T>C
ENST00000497666.1:n.97-1165T>C
ENST00000628224.2:c.3491T>C	ENSP00000487279.1:p.Met1164Thr
ENST00000633691.1:c.3155T>C	ENSP00000487724.1:p.Met1052Thr
NM_001135040.2:c.3482T>C	NP_001128512.1:p.Met1161Thr
NM_001135041.2:c.3140T>C	NP_001128513.1:p.Met1047Thr
NM_001190836.1:c.3431T>C	NP_001177765.1:p.Met1144Thr
NM_001190837.1:c.3536T>C	NP_001177766.1:p.Met1179Thr
NM_004082.4:c.3557T>C	NP_004073.2:p.Met1186Thr
NM_023019.3:c.3155T>C	NP_075408.1:p.Met1052Thr
NR_033935.1:n.3826T>C
NM_001135040.3:c.3482T>C	NP_001128512.1:p.Met1161Thr
NM_001135041.3:c.3140T>C	NP_001128513.1:p.Met1047Thr
NM_001190836.2:c.3431T>C	NP_001177765.1:p.Met1144Thr
NM_001190837.2:c.3536T>C	NP_001177766.1:p.Met1179Thr
NM_001378991.1:c.3506T>C	NP_001365920.1:p.Met1169Thr
NM_001378992.1:c.3488T>C	NP_001365921.1:p.Met1163Thr
NM_004082.5:c.3557T>C MANE Select	NP_004073.2:p.Met1186Thr
NM_023019.4:c.3155T>C	NP_075408.1:p.Met1052Thr
NR_033935.2:n.3605T>C