Canonical Allele Identifier: CA10616196

Gene: DCTN1

Linked Data

• ClinVar Variation Id: 337091
• ClinVar RCV Id: RCV000308960 ; RCV000347523 ; RCV002411237
• dbSNP Id: rs886056333
• MyVariant Identifiers: chr2:g.74597655T>A (hg19) ; chr2:g.74370528T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74370528T>A , CM000664.2:g.74370528T>A	GRCh38
NC_000002.11:g.74597655T>A , CM000664.1:g.74597655T>A	GRCh37
NC_000002.10:g.74451163T>A	NCBI36
NG_008735.2:g.26560A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361874.8:c.1065A>T	ENSP00000354791.4:p.Ala355=
ENST00000628224.3:c.1065A>T MANE Select	ENSP00000487279.2:p.Ala355=
ENST00000680606.1:c.1014A>T	ENSP00000505612.1:p.Ala338=
ENST00000361874.7:c.1065A>T	ENSP00000354791.3:p.Ala355=
ENST00000394003.7:c.1044A>T	ENSP00000377571.3:p.Ala348=
ENST00000409240.5:c.954A>T	ENSP00000386406.1:p.Ala318=
ENST00000409438.5:c.663A>T	ENSP00000387270.1:p.Ala221=
ENST00000409567.7:c.1005A>T	ENSP00000386843.3:p.Ala335=
ENST00000409868.5:c.1014A>T	ENSP00000387327.1:p.Ala338=
ENST00000434055.5:c.954A>T	ENSP00000416711.1:p.Ala318=
ENST00000466110.5:n.1286A>T
ENST00000628224.2:c.1014A>T	ENSP00000487279.1:p.Ala338=
ENST00000633691.1:c.663A>T	ENSP00000487724.1:p.Ala221=
NM_001135040.2:c.1005A>T	NP_001128512.1:p.Ala335=
NM_001135041.2:c.663A>T	NP_001128513.1:p.Ala221=
NM_001190836.1:c.954A>T	NP_001177765.1:p.Ala318=
NM_001190837.1:c.1044A>T	NP_001177766.1:p.Ala348=
NM_004082.4:c.1065A>T	NP_004073.2:p.Ala355=
NM_023019.3:c.663A>T	NP_075408.1:p.Ala221=
NR_033935.1:n.1266A>T
NM_001135040.3:c.1005A>T	NP_001128512.1:p.Ala335=
NM_001135041.3:c.663A>T	NP_001128513.1:p.Ala221=
NM_001190836.2:c.954A>T	NP_001177765.1:p.Ala318=
NM_001190837.2:c.1044A>T	NP_001177766.1:p.Ala348=
NM_001378991.1:c.1014A>T	NP_001365920.1:p.Ala338=
NM_001378992.1:c.996A>T	NP_001365921.1:p.Ala332=
NM_004082.5:c.1065A>T MANE Select	NP_004073.2:p.Ala355=
NM_023019.4:c.663A>T	NP_075408.1:p.Ala221=
NR_033935.2:n.1045A>T